PET and fMRI are relatively new techniques, which allows imaging of the brain without disturbing it, and they are important tools in clinical treatment and investigation. They are also used for cognitive investigation, by which I mean investigation the working of the healthy brain (Frackowiak et al, 1997). Naturally, the main focus of investigation is the cerebral cortex. In this paper, I survey the recent literature for evidence about the replicability of these studies. The survey covers 125 primary research articles, taken from 21 different journals during the first 10 months of 1997. The main findings are:
These findings suggest that there is a problem with replicability in cognitive imaging, and an effort is required to resolve it.
Cognitive imaging typically involve imaging the brains of the subjects in two experimental conditions, and comparing the activity of the brain in the two conditions. The regions in the brain where there is a different between the activity in the two conditions are then assumed to mark regions of cognitive processes that are different between the conditions.
An important assumption of cognitive imaging that underlies the interpretation of these studies is that when a differential activity shows in one study, it is replicable and hence generally applicable. In other words, it is expected that this differential activity is common to all healthy humans. This assumption is based on a more fundamental assumption, that humans have a common cognitive architecture, and that the cognitive imaging data reflects the characteristics of this architecture.
Is the assumption of replicability correct? In the words of one of papers in this survey (Schreus et al, 1997):" Replication is a necessary part of scientific investigation and it has met with variable success in PET. Investigations of seemingly similar paradigms do not often yield the same result." In this paper, I survey the literature for information about the replicability of cognitive imaging.
first, we need a clear idea what replication means in the context of cognitive imaging. The data that comes out of brain imaging studies is a set of small regions, with dimensions of few mm across, that are differentially active between the different experimental conditions. These are commonly called activations. In most of the cases, the actual data is the location of the peak of activity, in cartesian coordinates on a `standard' brain. Hence, a replication means finding the same activations in n a different study, using the same or closely related experimental paradigm. The `same activations' in the previous sentence have to be the majority of the activations, from two reasons:
Therefore, a match between two studies of a minority of the activations is at best a weak replication, and needs further testing before it can be taken as a proof for replicability in cognitive imaging.
In general, replicability is best tested by different research groups repeating the same experiment in a coordinated way, and then comparing the results. However, there is a lack of such studies in cognitive imaging. The only large study to investigate the replicability of cognitive imaging is the study by Poline et al(1996). In this study they compare the results from 12 European centres, in a very simple task. Their Figure 2 show the results from the 12 studies, and they clearly diverge. In particular, the area of activation ranges from almost nothing to almost all the anterior half of the left hemisphere. The authors say: "The high consistency between these patterns is seen clearly, especially among centers with high sensitivity", but the only similarity seen in their figure is the tendency for the cortical activation (the figure contain sub-cortical activation as well) to concentrate in the anterior half of the left hemisphere. The authors attribute this variability to different sensitivity of the machines in the different centers. In their conclusions, the authors say they found in the cortex three regions where almost all the studies have activation. However, to do that they:
Both of these manipulations increase a lot the chance of finding common activation. Since these manipulations are very different from the common practice in the field, the results cannot be used to estimate the replicability of the results of other studies. In the appendix to their paper. Poline et al(1997) give the coordinates of the peaks that were identified by each centre, at the threshold of p<0.05. The coordinates are presented in tables, with matching peaks between centres align together. Inspection of the table shows that there are no peaks where the majority of the centres have activation, and that the peaks distributions of different centres do not seem to relate to each other. The authors themselves say: "We observe large variability." They don't give any further analysis of this data.
Another comparative study is Poepple(1996), which compares the results of five studies of phonological processing, and says in his conclusion section: "In a comparison of five PET experiments on phonological processing that were very similar in their task demands, no overlap in results was found in local increases in rCBF across experiments." However, he does not discuss the overall problem of replicability of cognitive imaging. In their response (Demonet et al, 1996), the authors of these articles highlight the fact that all the studies show some activation in Broca area (their table 1), but they have to admit that outside Broca area the results diverge, and explain this by experimental variations.
Because of the lack of large studies to test the replicability of cognitive imaging, I decided to do a survey of the recent literature about replicability in cognitive imaging. The results of the survey are presented in the next section, followed by a section about possible explanations for the lack of replication that is seen in this survey, and an implications section.
In the survey, I included any research article or a review that I could find, which reports on cognitive imaging (by PET, fMRI or SPECT) in healthy humans, from the beginning of 1997 to the time of writing (October 1997). This is not meant to be an absolutely exhaustive cover of the literature at these period, but to be a representative sample of it. The survey included 125 research papers (excluding reviews), from 21 different journals, and these are marked by `**' in the references section.
In this survey I don't try to do any evaluation of the conclusions of these studies, or analyse the results, and I don't touch on the methodology of the data processing. The only thing I am looking for is evidence concerning replicability of cognitive imaging. In particular, I am looking for comparison of data between different studies, and Reports of success/failure to reproduce the results of other studies. Because, as will be seen below, these are very rare, I also look for comparison of data between individuals in the same study, assuming that this measure can give us hints about inter-study replication.
I divide the discussion to two major parts: one about replicability between studies, and the other about replicability between individuals in the same study. In addition, I also survey those reviews which specifically discuss cognitive imaging results in the same period, in a separate part.
In the 125 studies that I surveyed, there wasn't any report of a robust replication of the results of another study. The closest is the study by Hyder et al(1997), which compare their fMRI results with a previous PET study, and say:".., the agreement between the Talairach and Tournoux coordinates (18) for certain fMRI and PET activations is excellent. " However, out of 11 activations that they identify, only 3 match of the PET study, and of these one is 13.4mm away from the PET study and the second is 9.4mm (see their Table 2), which are clearly not `excellent match'. The authors also compare activations from a their own previous study and the same PET study (their Table 3), and here one activation (out of 5) matches. Thus in this study, we see, at best, a weak replication. Hyder et al (1997) do not present any analysis about the statistical probability of this match.
Only two other studies show data from different studies. Nobre et al(1997) show data from several studies in their figures 8 and 9. The data clearly diverge, and the authors say:"The variability in the reported loci of premotor activation in eye movement and visouspatial-attention studies is not negligible, and remains a point for further discussion and studies." Taylor et al(1997) show in their figure 5 results from five studies that used stroop stimuli, and these are also divergent. The authors comment on this figure is: "As is evident from inspection of Fig.5, reported ACC activations cover large extent of the cortex, and some of the apparent inconsistency may arise from a mistaken tendency to assume that foci separated by 2-3 cm represent the same function."
Three studies present coordinates of matches of an individual regions of activation. Zald and Padro (1997) find that the coordinates of a `weaker band' in their data match the activation in a previous PET study, but say nothing on the main areas of activations they found. Kanwisher et al(1997a) claim that the main peak which they found is close to peaks in previous similar studies, and quote the coordinates of almost identical peak in another study, but do not compare the rest of the activation in these studies. Orban et al(1997) pick matches to their results from the literature purely by matching coordinates, irrespective of the tasks that were used in these studies.
Two studies report failing to replicate the results of other studies, without presenting data. Kanwisher et al(1997b) compare their results to other studies, and find they do not match. They explain it by differences in the experimental settings. Dhankar et al(1997) report trying to reproduce the results of a previous study, which were unsuccessful.
Two studies report (without presenting actual data) replication of their own previous studies. Schreus et al(1997) claim that their study "replicates and expands our previous findings." However, later they say: "It is interesting to note that there some differences between the present study and our previous study," and go on to present a list of differences. These authors are clearly worried about the replicability of the results, because the next paragraph contains a discussion of replicability of PET studies, starting with the quote in the introduction above. In this discussion, they present two cases of discrepancies between studies, but none of replication. They go on to explain this by experimental variations. Jonides et al(1997) claim `excellent agreement' between the regions of activation in their study and in their own previous studies. However, they did the comparison using, in their words, a `relaxed criterion' of p<0.1, which is clearly not `excellent'.
The rest of the 116 studies either ignore completely the data of other studies, or compare it in qualitative terms, or compare the interpretation of the data (rather than the data itself).
There is one study showing data which shows robust replication within the subjects in the study. Binder et al(1997) divide the subjects in their study to two groups, and show data comparing the results of the two groups in their figure 4. The match is very good. However, Binder et al (1997) did not try to match their results with other studies.
Another example which looks good is in McCarthy et al(1997), which show in their figure 2 activation for faces from four subjects in one plane, which looks quite similar. However, the figure shows only four subjects out of 12, and only one plane. In Figure 3 they show activation for flowers from four subjects, and it is different.
fifteen other studies show data from more than one subject.
Gereon et al(1997) shows results from three subjects in their figure 1 and table 2. The data seems to cluster, but that is because the authors limited their data to the nonprimary motor areas. Within these areas, the data seems to be randomly distributed. The authors attribute at least some of the variability to variability in gyral morphology.
Carolee et al(1997) show data from 5 subjects in their figure 3 and 5. They highlight some regions of activation which are common to the five subjects, but from the figures it is clear that these regions are only small part of the activation in each individual brain. They do not present any analysis as to the probability of finding these common areas.
Nobre et al(1997) show images for pairs of subjects in their figures 1,2,3 and, 5, and they are clearly very different in each case.
Hyder et al(1997) say: "Activations of individual subjects were generally consistent with mean results, although the precise location of an activation within a gyrus varied, as can be seen in the anterior slice for two individual subjects shown in Fig.2." The activation in their figure 2, however, are not only `not precisely the same', they are completely different between the two individuals.
Kanwisher et al(1997a) show data from 12 subjects. However, they eliminated from their data subjects simply because they did not have activity in the region that Kanwisher et al(1997a) found. In addition, the presentation concentrate on this specific region, and ignore data about the rest of the brain. Kanwisher et al(1997a) is the only study that present data about the replicability of the results within the same individual over time. They show that for one subject, the results are very similar over a period of six months.
Tootell et al(1997) show data from four different subjects in their figure 8, showing the activation in the area V3A. As expected for such a low-level vision region, the activation is located more or less in the same place for all subjects, but there is still large variability between the subjects.
Gabrieli et al(1997) present data in their figure 2 from several subjects, but they use different plains through the brains, and not all the images are from the same experimental condition.
Wessinger et al(1997) show data from six subjects in their figure 2. As expected from a purely auditory task, the activation is concentrated in the auditory cortex, but inside this region it is different between the individuals. Wessinger et al say:" Clearly, there are individual differences, but the general pattern is the same: stimulus-specific differential activation is evidenced by the fact that the low-frequency and high-frequency representation overlay spatially different locations." i.e. the only similarity between individuals is that low- and high-frequency are different.
Bandettini et al(1997) show data from four subjects in their figure 2, and it is different between individuals. Clark et al(1997) show data from four subjects in their figure 1B, which show different activations (two subjects were excluded). Kraut et al(1997) show in their figure 2 data from two subjects, and it is different. Pugh et al(1997) show in their figure 4 data from two groups (one phonological sensitive vs. phonological insensitive) which is different.
Bavelier et al(1997) show data from 5 subjects in their figure 2, which displays a very large spread all over the cortex. The authors themselves say:"The comparison of individual patterns of activation across subjects revealed surprisingly large variability of the functional to anatomical mapping from one subject to another. While Broca's area was recruited in every subject, the fine localization of the activation with respect to the main sulci that characterizes this structure varied significantly between subjects."
Ye et al(1997) present in their figure 4 data from 7 subjects doing finger tapping. Even for such a simple motor activity, the activation pattern varies a lot between individuals.
Braver et al(1997) show data from nine subjects in their figure 4, which is very different in each individual. These author dedicate more than a page to a section called `Intersubject Variability'. However, in this section they do not analyse the variability, and do not consider the reasons for it or its implications.
Strother et al(1997) do not actually present data, but try to evaluate the reproducibility of the images between groups of subjects. Their results (their figure 1) show that, in the task that was used in their study, there is correlation between the activation images of groups of subjects. However, because they do not present the peaks of activity as other studies do, it is not possible to evaluate the relation between the correlation at the level of whole image (which Strother et al(1997) investigate) and the correlation of peaks of activation (which are reported by the rest of the studies).
The rest 108 studies present only average data or data from a single individual. It should be noted that Shulman et al(1997b, 1997c, 1997d) discuss replication, but a different kind of replication. In these studies, Both the hypothesis-generation and hypothesis-testing groups of tests are taken intentionally from the same group of subjects, and the replication is between tasks and between applications of the same task to the same subjects. 2c. Cognitive imaging reviews
I found small number of reviews which specifically discuss cognitive imaging results in the period of the survey. Most of these (Volkow et al 1997; Owen 1997; Smith &Jonides 1997; Friston 1997; Crammond 1997; Fletcher et al 1997; Fiez 1997) implicitly take replicability of cognitive imaging for granted. Two reviews actually compare data between different studies.
Cabeza & Nyberg (1997) review 73 studies. The review contains a section about caveats in cognitive imaging, but this does not contain discussion of replicability. They present data from these studies in their figures 1-7 The data clearly diverge, and give the impression of random distribution.
Bly and Kosslyn (1997) collect data from many studies about object recognition in their figure 1, and the data seems to be more or less randomly distributed in the posterior cortex. The authors themselves say there is a large variability. The authors discuss several possible explanations, and go as far as suggesting that object recognition is `opportunistic'' (by which they seem to mean 'variable in time').
The data about replication of cognitive imaging between different studies and different research groups is extremely sparse, and this sparse data is virtually all negative. Currently, there isn't even a single experimental paradigm which gives robust replication.
The data about replicability between individual subjects in the same study is also very sparse. It contains a single case of what looks like a robust replicability (Binder et al,1997), but the rest is also mostly negative.
Reviews mostly ignore the question of replication. The only review that discusses it (bly & Kosslyn, 1997) shows that the data is variable, and looks for an explanation. The other review that does shows data from different studies (Cabeza & Nyberg 1997) also shows large variability, without discussing it.
The survey in section 2 show a virtually absence of replication in cognitive imaging studies. Some possible explanations are mentioned in section 2, including variations in the experimental paradigm, differences between the machines that are used, and variability in gyral morphology. However, it is hard to see how these explanations can account for the virtual lack of replication, the failure to replicate in those studies that did try to do it (Kanwisher 1997a; Dhankher 1997), and the variability between subjects in the same study. These explanation could account for some failures of replication, but not for virtual absence of replication.
Moreover, even if these explanations are true, it does not solve the real problem of lack of replication. If the results of cognitive imaging are so sensitive to these artefacts, there is no way to know what part of the results is artefacts, and what part is real data.
The `opportunistic system' suggestion by Bly and Kosslyn (1997)(section 3c above) does seem good enough to explain the variability. In fact, this suggestion is quite extreme in its implications, because if it is true, we should not expect any replication ever, even between images of the same individual in different times. As mentioned in section (3b) above, I found only one case that reported about this possibility (Kanwisher et al,1997a), and they found replicability in the one subject they tested it on.
A less extreme suggestion is that the activation which is seen in cognitive imaging is replicable in each individual over time, but is variable between individuals, and hence between studies. In this case, the averaging in each study between the subjects picks up those activations that are shared by chance between significant proportion of the subjects in this study.
This intersubject variability can come from two non-mutually-exclusive reasons:
A weaker version of this possibility is that human has common cognitive architecture, but it is not associated with specific locations in the cortex. Since cognitive imaging gives us data about locations, this weaker version still means that cognitive imaging does not tell us a much the common architecture itself.
The lack of studies which explicitly try to replicate previous results make it impossible to conclude what is the reason for the lack of replication in cognitive imaging. However, the virtual lack of replication and the variability between individuals in the same study hints that it is a result of variability in the underlying data, rather than lack of effort for replication. A better answer to this point can be given only when more replication studies are published.
The survey in section 2 above clearly shows that there is lack of replication in cognitive imaging studies, and that there are potential problems with it. It is therefore essential to address this issue. Thus, must more effort should be made to replicate previous studies, and to report these results. These reports must be complete, and include both the matches and the non-matches. In addition, researchers should also check the replicability of the results in the same subjects over time, in particular to evaluate the `opportunistic system' suggestion of bly & Kosslyn (1997).
A common argument against this is that PET and fMRI equipment is expansive, and it is a waste of resources to re-do the same study again. However, if cognitive imaging gives us irreplicable data, it is a larger waste of resources. This is true even if only part of the studies are irreplicable, because currently we don't have a way to distinguish between good data (replicable results) and noise (irreplicable results). Thus it is essential to establish ways to distinguish between the good data and the noise.
In addition to more effort for replication, cognitive scientists should also consider the possibility that the lack of replication represent underlying variability, as discussed in section 3 above.
Allen, G., Buxton, R.B. Wong, E.C., & Courchesne, E.(1997). Attentional activation of the cerebellum independent of motor involvement. Science, 275, 1940-1943. **
Baker, S,C., Frith, C,D., & Dolan, R.J., (1997).The interaction between mood and cognitive function studied with PET. Psychological Medicine, 27, 565-578. **
Bäckman, L., Almkvist, O.,Andersson, J., Nordberg, A., Winblad, B., Reineck, R., & Langström, B. (1997). Brain activation in young and older adults during implicit and explicit retrieval. Journal of Cognitive Neuroscience, 9, 378-391. **
Bandettini, P.A., Kwong, K.K., Davis, T.L., Tootell, R.B.H., Wong, E.C., Fox, P.T., Belliveau, J.W., Weisskoff, R.M., & Rosen, B.R.(1997). Characterization of cerebral blood oxygenation and flow changes during prolonged brain activation. Human Brain Mapping, 5, 93-109. **
Bavelier, D., Corina, D., Jezzard, P., Padmanabhan, S., Clark, P., Karni, A., Prinster, A., Braun, A., Lalwani, A., Rauschecker, J.P., Turner, R., & Neville, H. (1997) Sentence Reading: A functional MRI study at 4 Tesla. Journal of Cognitive Neuroscience, 9, 664-686. **
Beauchamp, M.S., Cox, R.W., & DeYoe, E.A.(1997). Graded effects of spatial and featural attention on human area MT and associated motion processing areas. Journal of Neurophysiology, 78, 516-520. **
Beauregard, M., Chertkow, H., Bub, D., Murtha, S., Dixon, R., Evans, A.(1997). The neural substrate for concrete, abstract, and emotional word lexicon. A Positron Emission Tomography study. Journal of Cognitive Neuroscience, 9, 441-461. **
Berman, K.F., Schmidt, P.J., Rubinow, D.R., Danaceau, M.A., Van Horn, J.D., Esposito, G., Ostrem, J.L., & Weinberger, D.R.(1997). Modulation of cognition-specific cortical activity by gonadal steroids: A positron-emission tomography study in women. Proceeding of the National Academy of Science, 94, 8836-8841. **
Binder, J.R., Frost, J.A., Hammeke, T.A., Cox, R.W., Rao, S.M., & Prieto, T.(1997). Human brain language areas identified by functional magnetic resonance imaging. Journal of Neuroscience, 17, 353-362. **
Blok, B.F.M., Willemsen, A.T.M., & Holstege, G., (1997). A PET study on brain control of micturition in humans. Journal of Cognitive Neuroscience, 9, 111-121. **
Bly, B.M., & Kosslyn, S.M.(1997). Functional anatomy of object recognition in humans: evidence from positron emission tomography and functional magnetic imaging. Current Opinion in Neurology, 10, 5-9.
Bodis-Wollner, I., Bucher, S.F., Seelos, K.C., Paulus, W., Reiser, M., & Oertel W.H. (1997). Functional MRI mapping of occipital and frontal cortical activity during voluntary and imagined saccades. Neurology, 49, 416-420. **
Braun, A.R., Balkin, T.J., Wesensten, N.J., Carson, R.E., Varga, M., Baldwin, P., Selbie, S., Belenky, G., & Herscovitch, P.(1997). Regional cerebral blood flow throughout the sleep-wake cycle. An H215O study. Brain, 120, 1173 - 1197. **
Braver, T.S., Cohen, J.D., Nystrom, L.E., Jonides, J., Smith, E.E., Noll, D.C. (1997). A parametric study of prefrontal cortex involvement in human working memory. NeuroImage, 5, 49-62. **
Brodal, P. (1992) The Central Nervous System: structure and function. Oxford, UK: OUP.
Burton, H., MacLeod, A-M.K., Videen, T.O., & Raichle, M.E.(1997). Multiple foci in parietal and frontal cortex activated by rubbing embossed grating patterns across fingerpads: a positron emission tomography study in humans. Cerebral Cortex, 7, 3-17. **
Busatoo, G., Howard, R.J., Ha, Y., Bramner, M., Wright, I.,Woodruff, P.W.R., Simmons, A., Williams, S.C.R., David, A.S., & Bullmore, E.T.(1997). A fMRI study of episodic memory. Neuroreport, 8, 2671-2675. **
Cabeza, R., & Nyberg, L.(1997). Imaging cognition: An empirical review of pet studies with normal subjects. Journal of Cognitive Neuroscience, 9, 1-26.
Cabeza, R., Kapur, S., Craik, F.I.M., McIntosh, A.R., Houle, S., &Tulving, E. (1997a). Functional Neuroanatomy of Recall and Recognition: A PET study of episodic memory. Journal of Cognitive Neuroscience, 9, 254-265. **
Cabeza, R., Grady, C.L., Nyberg, L.,McIntosh, A.R.,Tulving, E., Kapur, S., Jennings, J.M., Houle, S., Craik, F.I.M.(1997b). Age-related differences in neural activity during memory encoding and retrieval: A Positron Emission Tomography study. Journal of Neuroscience, 17, 391-400. **
Calvert, G.A., Bullmore, E.T., Brammer, M.J., Campbell, R., Williams, S.C., McGuire, P.K., Woodruff, W., Iversen, S.D., & Dav, A.S.(1997). Activation of auditory cortex during silent lipreading. Science, 276, 593-596. **
Clark, V.P., Parasuraman, R., Keil, K., Kulansky, R., Fannon, S., Maisong, J.M., Ungerleider, L.G., Haxby, J.V. (1997). Selection attention to face identity and color studied with fMRI. Human Brain Mapping, 5, 293-297. **
Coull, J.T., Frith, C.D., Dolan, R.J., Frackowiak, R.S.J., & Grasby, P.M.(1997). The neural correlates of the noradrenergic modulation of human attention, arousal and learning. The European Journal of Neuroscience, 9, 589 - 598. **
Courtney, S.M., Ungerleider, L.G., Keil, K., & Haxby, J.V.(1997). Transient and sustained activity in a distributed neural system for human working memory. Nature, 386, 608-612. **
Courtney, S.M., & Ungerleider, L.G.(1997). What fMRI has taught us about human vision. Current Opinion In Neurobiology, 7,554-561.
Crammond, D.J.(1997). Motor imaginary: never in your wildest dreams. Trends in neuroscience, 20,54-57.
Davis, K.D., Taylor, S.J., Crawley, A.P., Wood, M.L., & Mikulis, D.J.(1997). Functional MRI of pain and attention related activation in the human cingulate cortex. Journal of Neurophysiology, 77, 3370-3380. **
Decety, J., Grezes, J., Costes, N., Perani, D., Jeannerod, M., Procyk, E., Grassi, F., & Fazio, F. (1997). Brain activity during observation of actions. Influence of action content and subject's strategy. Brain, 120, 1763-1777. **
Deiber, M.P., Wise, S.P., Honda, M., Ctatalan, M.J., Grafman, J., & Hallett, M.(1997). Frontal and Parietal networks for conditional motor learning: a PET study. Journal of Neurophysiology, 78, 977-991. **
DeMeyer, W. (1988) Neuroanatomy. Harwell Publishers.
Demonet, J.F., Fiez, J.A., Paulesu, E., Petersen, S.E., & Zatore. R.J.(1996). REPLY. Brain and Language, 55, 352-379.
Dhankher, A., Wexler, B.E., fulbright, R.K., Halwes, T., Blamire, A.M., & Shulman, R.G.(1997). fMRI assessment of the human brain auditory cortex response to increasing word presentation rate. Journal of Neurophysiology, 77, 476-483. **
Dolan, R.J., & Fletcher, P.C.(1997). Dissociating prefrontal and hippocampal function in episodic memory encoding. Nature, 388,582-587. **
Dolan, R.J., Fink, G.R., Rolls, E., Booth, M., Holmes, A., Frackowiak, R.S.J., & Friston, K.J., (1997). How the brain learn to see objects in an impoverished context. Nature, 389, 596-599.**
Endo, S., Toyama, H., Kimura, Y., Ishii, K., Senda, M., Kiyosawa, M., &Uchiyama A. (1997). Mapping visual field with positron emission tomography by mathematical modelling of the retinotopic organization in the calcarine cortex. IEEE Transactions of Medical Imaging 16, 252-60. **
Engel, S.A.,Glover, G.H., &Wandell, B.A.(1997a). Retinotopic organization in human visual cortex and the spatial precision of functional MRI. Cerebral Cortex, 7,181-192. **
Engel, S., Zhang, X., & Wandell, B.(1997b). Colour tuning in human visual cortex measured with fMRI. Nature, 388, 68-71. **
Faillenot, I., Sekuta, H., couter, N., decety, J., & Jeannerod, M. (1997a). Visual working memory for shape and 3d-orientation: a PET study. Neuroreport, 8, 859-862. **
Faillenot, I., Toni I., Decety, J., Gregoire, M-C., & Jeannerod, M.(1997b). Visual pathways for object-oriented action and object recognition: functional anatomy with PET. Cerebral Cortex, 7, 77 - 85. **
Fiez, J.A. (1997). Phonology, semantics, and the role of the left inferior prefrontal cortex. Human Brain Mapping, 5, 78-93.
Fink, G.R., Frackowiak, R.S.J., Pietryzk, U., & Passingham, R.E. (1997a). Multiple nonprimary motor areas in the human cortex. Journal of Neurophysiology, 77, 2164-2174. **
Fink, G.R., Halligan, P.W., Marshall, J.C., Frith, C.D., Frackowiak, R.S.J., & Dolan R.J. (1997b). Neural mechanisms involved in the processing of global and local aspects of hierarchically organized visual stimuli. Brain, 120, 1779-1791. **
Fink, G.R., Marshall, J.C., Halligan, P.W., Frith, C.D., Frackowiak, R.S., &Dolan, R.J. (1997c). Hemispheric specialization for global and local processing: the effect of stimulus category. Proceeding of the Royal Society of London B: Biological Sciences, 264, 487-94. **
Fletcher, P.C., Frith, D.D., & Rugg, M.D.(1997). The functional neuroanatomy of episodic memory. Trends in neuroscience, 20, 213-218.
Fox, P., Ingham, R., George, M.S., Mayberg, H., Ingham, J., Roby, J., Martin, C., & Jerabek, P.(1997). Imaging human intra cerebral connectivity by PET using TMS. Neuroreport, 8, 2787-2791. **
Frackowiak, R., Friston, K.J, Frith, C.D., Dolan, R. (1997). Human Brain Function. San-Diego, CA: Academic Press.
Friston, K.J.(1997). Imaging cognitive anatomy. Trends in cognitive sciences, 1,21-27.
Frith, C.D., & Dolan, R.J.(1997). Brain mechanisms associated with top-down processes in perception. The Royal Society Philosophical Transactions: Biological Sciences B, 352,1221-1230.
Fujii, J., Okuda, J., Kawashima, R., Yamadori, A., Fukatsu, R., Suzuki, K., Ito, M., Goto, R., & Fukuda, H.(1997). Different roles of the left and right parahippocampal regions in verbal recognition: a PET study. Neuroreport, 8, 1113-1117. **
Furey, M.L., Pietrini, P., Haxby, J.V., Alexander, G.E., Lee, H.C., VanMeter, J., Grady, C.L., Shetty, U., Rapoport, S.I., Schapiro, M.B., & Freo, U.(1997). Cholinergic stimulation alters performance and task-specific regional cerebral blood flow during working memory. Proceeding of the National Academy of Science, 94, 6512-6516. **
Gabrieli, J.D., Brewer, J.B., Desmond, J.E., Glover, G.H.(1997). Separate neural bases of two fundamental memory processes in the human medial temporal lobe. Science, 276,264-266. **
Goel, V., Gold, B., Kapur, S., & Houle, S.(1997). The seats of reason? An imaging study of deduction and induction reasoning. Neuroreport, 8, 1305-1310. **
Guathier, I., Anderson, A.W., Tarr, M.J., Skudlarsky, P., & Gore, J.C.(1997). Levels of categorization in visual recognition studied using functional MRI. Current Biology, 7,645-651. **
Gur, R.C., Ragland, J.D., Mozley, L.H., Mozley, P.D., Smith, R., Alavi, A., Bilker, W., & Gur, R.E.(1997). Lateralized changes in regional cerebral blood flow during performance of verbal and facial recognition tasks: correlation with performance and "effort." Brain and Cognition, 33, 388-444. **
Hazeltine, H., Grafton, S.T., & Ivry, R.(1997). Attention and stimulus characteristics determine the locus of motor-sequence encoding. A PET study. Brain, 120, 123 - 140. **
Herbster, A.N., Mintun, M.A., Nebes, R.D., & Becker, J.T.(1997). Regional cerebral blood flow during word and nonword reading. Human Brain Mapping, 5, 84-92. **
Hillyard, S.A., Hinrichs, H., Templemann, C., Morgan, S.T., Hansen, J.C., Scheic, H., & Heinze, H-J.(1997). Combining steady-state visual evoked potentials and fMRI to localize brain activity during selective attention. Human Brain Mapping, 5, 287-292. **
Hirano, S., Kojima, H., Naito, Y., Honjo, I., Kamoto, Y., Okazawa, H., Ishizu, K., Yonekura, Y., Nagahama, Y., Fukuyama, H., & Kehishi, J.(1997). Cortical processing mechanism for vocalization with auditory verbal feedback. Neuroreport, 8, 2379-2382. **
Hofle, N., Paus, T., Reutens, D., Fiset,P., Gotman, J., Evans, A.C., & Jones, B.E.(1997). Regional Cerebral Blood Flow changes as a function of delta and spindle activity during slow wave sleep in humans. Journal of Neuroscience, 17, 4800-4808. **
Humphrey, G.K., Goodale, M.A., Bowen, C.V., Gati, J.S., Vilis, T., Rutt, B.K., & Menon, R.S. (1997). Differences in perceived shape from shading correlate with activity in early visual areas. Current Biology, 7, 144-147. **
Hyder, F., Phelps, E.A.,Wiggins, C.J., Labar, K.S., Blamire, A.M., & Shulman, R.G.(1997). "Willed action": A functional MRI study of the human prefrontal cortex during a sensorimotor task. Proceeding of the National Academy of Science, 94, 6989-6994. **
Iacoboni, M., Woods, R.P., Lenzi, G.L., & Mazziotta, J.C.(1997). Merging of oculomotor and somatomotor space coding in the human right precentral gyrus. Brain, 120, 1635 - 1645. **
Imaizumi, S., Mori, K., Kiritani, S., Kawashima, R., Sugiura, M., Fukuda, H., Itoh, K., Kato, T., Nakamura, A., Hatano, K., Kojima, S., Inakamura, K.(1997). Vocal identification of speaker and emotion activates different brain regions. Neuroreport, 8, 2809-2812. **
Indefrey, P., Kleinschmidt, A., Merboldt, K.-D., Kruger, G., Brown, C., Hagoort, P., & Frahm. J. (1997) (Note). Equivalent responses to lexical and nonlexical visual stimuli in occipital cortex: a functional magnetic resonance imaging study. NeuroImage, 5, 78-81. **
Jennings, J.M., McIntosh, A.R., Kapur, S., Tulving, E., & Houle, S. (1997). Cognitive substraction may not add up: the interaction between semantic processing and response mode. NeuroImage, 5, 229-239. **
Johannsen, P., Jakobson, J., Bruhn, P., Hansen, S.B., Gee, A., Stodkilde-jorgensen, H., & Gjedde, A. (1997). Cortical sites of sustained and divided attention in normal elderly humans. NeuroImage, 6, 145-155. **
Jonides, J., Schumacher, E.H., Smith, E.E., Lauber, E.J., Awh, E., Minoshima, S., &Koeppe, R.A.(1997). Verbal Working Memory Load Affects Regional Brain Activation as Measured by PET. Journal of Cognitive Neuroscience, 9, 462-475. **
Jueptner, M., Stephan, K.M., Frith, C.D., Brooks, D.J., Frackowiak, R.S.J., & Passingham, R.E. (1997a). Anatomy of motor learning: I. Frontal cortex and attention to action. Journal of Neurophysiology, 77, 1313-1324. **
Jueptner, M., Frith, C.D., Brooks, D.J., Frackowiak, R.S.J., & Passingham, R.E. (1997b). Anatomy of motor learning: II. Subcortical structures and learning by trial and error. Journal of Neurophysiology, 77, 1325-1337. **
Kanwisher, N., McDermott, J., & Chun, M.M.(1997a). The fusiform face area: A module in human extrastriate cortex specialized for face perception. Journal of Neuroscience, 17, 4302-4311. **
Kanwisher, N., Woods, R.P., Iacoboni, M., & Mazziotta, J.C,(1997b). A locus in human extrastriate cortex for visual shape analysis. Journal of Cognitive Neuroscience, 9, 133-142. **
Kawashima, R., Inoue, K., Sato, K., & Fukuda, H.(1997). Functional symmetry of cortical motor control in left handed subjects. Neuroreport, 8, 1729-1732. **
Kilinberg, T., O'Sullivan, B.T., & Roland, P.E.(1997). Bilateral activation of fronto-parietal networks by incrementing demand in a working memory test. Cerebral Cortex, 7,465-471. **
Kim, K.H.S., Melkin, N.R.,Lee, K-M., & Hirsch, J.(1997). Different cortical areas associated with native and second languages. Nature, 388, 171-174. **
Kraut, M., Hart, J. Jr., Soher, B.J. & Gordon, B. (1997). Object shape processing in the visual system evaluated using functional MRI. Neurology, 48,1416-20. **
Maguire, E.A., Frackowiak, R.S.J., & Frith, C.D.(1997). Recalling routes around London: Activation of the right hippocampus in taxi drivers. Journal of Neuroscience, 17, 7103-7110. **
Mangun, G.R., Hopfinger, J.B., Kussmaul, C.L., Fletcher, E.M., Heinze, H-J.(1997). Covariations in ERP and PET measures of spatial selective attention in human extrastriate visual cortex. Human Brain Mapping, 5, 273-279. **
Maquet, P., Degueldre, C., Delfiore, G., Aerts, J., Péters, J-M., Luxen, A., & Franck, G.(1997). Functional neuroanatomy of human slow wave sleep. Journal of Neuroscience, 17, 2807-2812. **
Marshall, R.S., Lazar, R.M., Van Heertum, R.L., Esser, P.D., Perera, G.M., & Mohr, J.P. (1997). Changes in regional cerebral blood flow related to line bisection discrimination and visual attention using HMPAO-SPECT. NeuroImage, 6, 139-144. **
Martinez, A., moses, P., Frank, L., Buxton, R.,Wong, E., & Stiles, J.(1997). Hemispheric asymmetry in global and local processing: evidence from fMRI. Neuroreport, 8, 1685-1689. **
McCarthy, G., Luby, M., Gore, J., & Goldman-Rakic, P.(1997a). Infrequent events transiently activate human prefrontal and parietal cortex as measured by fMRI. Journal of Neurophysiology, 77, 1630-1634. **
McCarthy, G., Puce, A., Gore, J.C., & Allison, T. (1997b). Face-specific processing in the human fusiform gyrus. Journal of Cognitive Neuroscience, 9, 605-610. **
Mcguire, P.K., Robertson, D., Thacker, A., David, A.S., Kitson, N., Frackowiak, R.S.J., & Frith, C.D.(1997). Neural correlates of thinking in sign language.Neuroreport, 8, 695-698. **
McIntosh, A.R., Nyberg, L., Bookstein, F.L., & Tulving, E. (1997). Differential functional connectivity of prefrontal and medial temporal cortices during episodic memory retrieval. Human Brain Mapping, 5, 323-327. **
McKeefry, D.J., Watson, J.D.G., Frackowiak, R.S.J., Fong, K., Zeki, S. (1997). The activity in human area V1/V2, V3, and V5 during the perception of coherent and incoherent motion. NeuroImage, 5,1-12. **
Lacquaniti, F., Perani, D., Guigon, E., Bettinardi, V., Carrozzo, M., Grassi, F., Rossetti, Y., & Fazio, F. (1997). Visuomotor transformation for reaching to memorized targets: a PET study. NeuroImage, 5, 129-146. **
Menon, R.S., Ogawa, S., Strupp, J.P., & Ugurbil, K. (1997). Ocular dominance in human V1 demonstrated by functional magnetic resonance imaging. Journal of Neurophysiology, 77, 2780-2787. **
Mentis, M.J., Alexander, G.E., Grady, C.L., Horwitz, N., Krasuski, J., Pietrini, P., Strassburger, T., Hampel, H., Schapiro, M.B., & Rapaport, S.I. (1997). Frequency variation of a pattern-flash visual stimulus during PET differentially activates brain from striate through frontal cortex. NeuroImage, 5, 116-128. **
Morris, J.S., Friston, K.J., & Dolan, R.J.(1997). Neural responses to salient visual stimuli. Proceeding of the Royal Society of London B: Biological Sciences, 264, 769-775. **
Nobre, A.C., Sebestyen, G.N., Gitelman, D.R., Mesulam, M.M., Frackowiak, R.S.J., & Frith, C.D.(1997). Functional localization of the system for visuospatial attention using positron emission tomography. Brain, 120, 515 - 533. **
Nolte, J. (1993). The human brain (third edition). St Louis, Missouri: Mosby-Year book, Inc.
Orban, G.A., Dupont, P., Vogels, R., Bormans, G., & Mortelmans, L.(1997). Human brain activity related to orientation discrimination tasks. The European Journal of Neuroscience, 9, 246 - 259. **
Owen, A.M.(1997). Mini-review. The functional organization of working memory processes within human lateral frontal cortex: the contribution of functional neuroimaging. The European Journal of Neuroscience, 9, 1329 - 1339.
Paulesu, E., Goldacre, B., Scifo, P., Cappa, S.E., Gilardi, M.C., Castiglioni, I., Perani, D., & Fazio, F.(1997). Functional heterogeneity of left inferior frontal cortex as revealed by fMRI. Neuroreport, 8, Neuroreport, 8, 2011-2016. **
Paus, T., Jech, R., Thompson, C.J., Comeau, R., Peters, T., & Evans, A.C.(1997a). Transcranial magnetic stimulation during Positron Emission Tomography: A new method for studying connectivity of the human cerebral cortex. Journal of Neuroscience, 17, 3178-3184. **
Paus, T., Zatorre, R.J, Hofle, N., Caramanos, Z.,Gotman, J.,Petrides, M., & Evans, A.C.(1997b). Time-related changes in neural systems underlying attention and arousal during the performance of an auditory vigilance task. Journal of Cognitive Neuroscience, 9, 392-408. **
Perlstein, W.M., Braver, T.S., Nystrom, L.E., Noll, D.C., Jonides, J., Smith, E. E., & Cohen, J. D. (1997). Temporal dynamics of brain activation during a working memory task. Nature, 386, 604-608. **
Peterson, K.M., Elfgren, C., & Ingver, M. (1997). A dynamic role of the medial temporal lobe during retrieval of declarative memory in man. NeuroImage, 6, 1-122. **
Petit, L., Clark, V.P., Ingeholm, J., & Haxby, J.V.(1997). Dissociation of saccade-related and pursuit-related activation in human frontal eye fields as reveal by fMRI. Journal of Neurophysiology, 77, 3386-3390. **
Phillips, M.L., Young, A.W., Senior, C., Brammer, M., Andrew, C., Calder, A.J., Bullmore E.T., Perrett,D.I., Rowland, D., Williams, S.C.R., Gray, J.A., & David, A.S. (1997). A specific neural substrate for perceiving facial expression of disgust. Nature, 389, 495-499. **
Platel, H., Price, C. Baron, J-C., Wise, R., Lambert, J., Frackowiak, R.S.J., Lechevalier, B., Eustache, F.(1997). The structural components of music perception. A functional anatomical study. Brain, 120, 229 - 243. **
Poepple, D.(1996). A critical review of PET studies of phonological processing. Brain and Language 55, 317-371.
Poline, J-B., Vandenberghe, R., Holmes, A.P., Friston, K.J., & Frackowiak, R.S.J. (1996). Reproducibility of PET activation studies: lessons from a multi-center European experiment. NeuroImage 4, 34-54.
Price, C.J., & Friston, K.J.(1997). Cognitive conjunction: a new approach to brain activation experiments. NeuroImage, 5, 261-270. **
Pugh, K.R., Shaywitz, B.A., Shaywitz, S.E., Shankweiler, D.P., Katz, L., Fletcher, J.M., Skudlarski, P., Fulbright, R.K., Constable, R.T., Bronen, R.A., Lacadie, C., & Gore, J.C.(1997). Predicting reading performance from neuroimaging profiles: the cerebral basis of phonological effects in printed word identification. Journal of Experimental Psychology: Human Perception and Performance 23,299-318. **
Prbhakarana, V., Smith, J.A.L., Desmond, J.E., Glover, G.H., Gabrieli, J.D.E.(1997). Neural subtrates of fluid reasoning: an fMRI study of neocortical activation during performance of the Raven's progressive matrices test. Cognitive Psychology 33, 43-63. **
Price, C.J., Morre, C.J., & Friston, K.J. (1997). Substructions, conjunctions, and interactions in experimental design of activation studies. Human Brain Mapping, 5, 264-272. **
Ragland, J.D., Rahlan, D.C., Gur, R.C., Censits, D.M., Smith, R.J., Mozley, P.D., Alavi, A., & Gur, R.E.(1997). PET regional cerebral blood flow during working memory and declarative memory: Relationship with task performance. Neuropsychology 11,2222-2310. **
Reppas, J.R., Niyogi, S., Dale, A.M., Sereno, M.I., & Tootell, R.B.H.(1997). Representation of contour boundaries in retinotopic human visual cortical areas. Nature, 388,175-179. **
Rainville, P., Duncan, G.H., Price, D.D., Carrier, B., & Bushnell, M.C.(1997). Pain affect encoded in human anterior cingulate but not somatosensory cortex. Science, 277, 968-970. **
Rao, S.M., Bobholz, J.A., Hammeke, T.A., Rosen, A.C., Woodley, S.J., Cunningham, J.M., Cox, R.W., Stein, E.A., & Binder, J.R.(1997a). Functional MRI evidence for subcortical participation in conceptual reasoning skills. Neuroreport, 8, 1987-1993. **
Rao, S.M., Harrington, D.L., Haaland, K.Y., Bobholz, J.A., Cox, R.W., & Binder, J.R.(1997b). Distributed neural systems underlying the timing of movements. Journal of Neuroscience, 17, 5528-5535. **
Rauch, S.L., Whalen, P.J., Savage, C.R., Curran, T., Kendrick, A.A., Brown, H.D., Bush, G., Breiter, H.C., & Rosen, B.R. (1997). Striatal recruitment during an implicit sequence learning task as measured by functional magnetic resonance imaging. Human Brain Mapping, 5, 124-132. **
Rees, G., Frackowiak, R.S.J., & Frith, C.(1997). Two modulatory effects of attention that mediate object categorization in human cortex. Science, 275, 835-838. **
Richter, W., Andersen, P.M., Georgopoulos, A.P., & Kim, S-G.(1997). Sequential activity in human motor areas during a delayed cued finger movement task studied by time resolved MRI. Neuroreport, 8, 1257-1261. **
Rosier, A., Cornette, L., Dupont, P., Bormans, G., Michiels, J., Mortelmans, L., Orban, G.A.(1997). Positron Emission Tomography imaging of long term shape recognition challenges. Proceeding of the National Academy of Science, 94, 7627-7632. **
Rugg, M.D., Fletcher, F.C.,Frith, C.D., Frackowiak, R.S.J., & dolan, R.J.(1997). Brain regions supporting intentional and incidental memory: a PET study. Neuroreport, 8, 1283-1287. **
Rumsey, J.M., Horwitz, B., Donohue, B.C., Nace, K., Maisog, J.M., & Andreason, P. (1997). Phonological and orthographic components of word recognition. A PET-rCBF study. Brain, 120, 739-759. **
Sahraie, A., Weiskrantz, L., Barbur, J.L., Simmons, A., Williams, S.C.R., & Brammer, M.J.(1997). Pattern of neuronal activity associated with conscious and unconscious processing of visual signals. Proceeding of the National Academy of Science, 94, 9406-9411. **
Schreus, B.G., McIntosh, A.R., Bahro, M., Herscovitch, P., sunderland, T., & Molchan, S.E.(1997). Lateralization and behavioural correlation of changes in regional cerebral blood flow with classical conditioning of the human eyeblink response. Journal of Neurophysiology, 77, 2153-2163. **
Seitz, R.J., Canavan, A.G.M., Yaguez, L., Herzog, H., Tellmann, L., Knorr, U., Huang Y., & Homberg, V.(1997). Representations of graphomotor trajectories in the human parietal cortex: evidence for controlled processing and automatic performance. The European Journal of Neuroscience, 9, 378 - 389. **
Shadmehr, R., & Holcomb, H.H.(1997). Neural correlates of motor memory consolidation. Science, 277,821-825. **
Shulman, G.L.,Corbetta, M.,Buckner, R.L.,Raichle, M.E.,Fiez, J.A.,Miezin, F.M., & Petersen, S.E.(1997a). Top-down modulation of early sensory cortex. Cerebral Cortex, 7,193 - 206. **
Shulman, G.L., Corbetta, M., Fiez, J.A., Buckner, R.L., Miezin, F.M., Raichle, M.E., & Petersen, S.E. (1997b). Searching for activations that generalize over tasks. Human Brain Mapping, 5, 317-322. **
Shulman, G.L., Corbetta, M., Buckner, R.L., Fiez, J.A., Miezin, F.M., Raichle, M.E., & Petersen, S.E. (1997c). Common blood flow changes across visual tasks: I. Increases in subcortical structures and cerebellum but not in nonvisual cortex. Journal of Cognitive Neuroscience, 9, 624-647. **
Shulman, G.L., Corbetta, M., Buckner, R.L., Fiez, J.A., Miezin, F.M., Raichle, M.E., & Petersen, S.E. (1997d). Common blood flow changes across visual tasks: II. Decreases in cerebral cortex. Journal of Cognitive Neuroscience, 9, 648-663. **
Smith E.E., & Jonides J. (1997). Working memory: a view from neuroimaging. Cognitive Psychology, 33,5-42.
Soderfeldt, B., Ingvar, M., Ronnberg, J., Eeriksson, L., Serrander, M., & Stone-Elander, S.(1997). Signed and spoken language perception studied by positron emission tomography. Neurology, 59, 82-87. **
Strother, S.C., Lange, N., Anderson, J.R., Schaper, K.A., Rehm, K., Hansen, L.K., Rottenberg, D.A. (1997). Activation pattern reproducibility: measuring the effects of group size and data analysis models. Human Brain Mapping, 5, 312-316.
Svensson, P., Minoshima, S., Beydoun, A., Morrow, T.J., & Casey, K. (1997). Cerebral processing of acute skin and muscle pain in humans. Journal of Neurophysiology, 78, 7450-7460. **
Tagaris, G.A, Kim, S-G., Strupp, J.P., Andersen, P., Ugurbil, K., & Georgopoulos, A.P.(1997). Mental rotation studied by Functional Magnetic Resonance Imaging at high field (4 Tesla): Performance and Cortical Activation. Journal of Cognitive Neuroscience, 9, 419-432. **
Taylor, S.F., Kornblum, S., Lauber, E.J., Minoshima, S., & Koeppe, R.A. (1997). Isolation of specific interference processing in the stroop task: PET activation studies. NeuroImage, 6, 81-92. **
Thut, G., Schultz, W., Roelcke, U., Nienhusmeier, M., Missimer, J., Maguire, R.P., & Leenders, K.L. (1997). Activation of the human brain by monetary reward. Neuroreport, 8, 1225-1228. **
Tootell, R.B.H., Mendola, J.D., Hadjikhani, N.K., Ledden, P.J., Liu, A.K., Reppas, J.B., Sereno, M.I., & Dale, A.M.(1997). Functional analysis of V3A and related areas in human visual cortex. Journal of Neuroscience, 17, 7060-7078. **
Tzourio, N., El Massioui, F., Crivello, F., Joliot, M., Renault, B., & Mazoyer, B. (1997). Functional anatomy of human auditory attention studied with PET. NeuroImage, 5, 63-77. **
Vandenberghe, R., Duncan, J., Dupont, P., Ward, R., Poline, J-B. Bormans, G., Michiels, J., Mortelmans, L., & Orban, G.A.(1997). Attention to one or two features in left or right visual field: A Positron Emission Tomography study. Journal of Neuroscience, 17, 3739-3750. **
Van Oostende, S., Van Hecke, P., Sunaert, S., Nuttin, B., & Marchal, G. (1997). fMRI studies of the supplementary motor area and the premotor cortex. NeuroImage, 6, 181-190. **
Volkow, N.D., Rosen, B., & Farde, L.(1997). Imaging the living human brain: Magnetic resonance imaging and positron emission tomography. Proceeding of the National Academy of Science, 94, 2787-2788.
Wessinger, C.M., Buonocore, M.H., Kussmaul, C.L., & Mangun, G.R.(1997). Tonotopy in human cortex examined with functional magnetic resonance imaging. Human Brain Mapping, 5, 18-25.**
Wilkinson, J.E. (1992) Neuroanatomy for medical students (2nd edition). Oxford, UK: Butterworth-Heinmann Ltd.
Winstein, C.J., Grafton, S.T., & Pohl, P.S.(1997). Motor task difficulty and brain activity: Investigation of goal directed reciprocal aiming using PET. Journal of Neurophysiology, 77, 1581-1594. **
Woldorff, M.G., Fox, P.T., Matzke, M., Lancaster, L.L., Veeraswamy, S., Zamarripa, F., Seabolt, M., Glass, T., Gao, J.H., Martin, C.C., & Jerabek, P.(1997). Retinotopic organization of early visual spatial attention effects as revealed by PET and ERPs. Human Brain Mapping, 5, 280-286. **
Ye, F.Q., Smith, A.M., Yang, Y., DUYN, J., Mattay, V.S., Ruttimann, U.E., Frank, J.A., Weinberger, D.R., & McLaughlin, A.C.(1997). Quantitation of regional cerebral blood flow increases during motor activation: a steady-state arterial spin tagging study. NeuroImage, 6, 104-112. **
Zald, D.H., & Pardo, J.V.(1997). Emotion, olfaction, and the human amygdala: Amygdala activation during aversive olfactory stimulation. Proceeding of the National Academy of Science, 94, 4119-4124. **