Galit Yovel

Neural correlates of the left-visual-field superiority in face perception appear at multiple stages of face processing.

Facilitation and disruption of lateralized syllable processing by unattended stimuli in the opposite visual field.

The neural basis of the butcher-on-the-bus phenomenon: when a face seems familiar but is not remembered.

Face perception: domain specific, not process specific.

The neural basis of the behavioral face-inversion effect.

Specialized face perception mechanisms extract both part and spacing information: evidence from developmental prosopagnosia.

The fusiform face area: a cortical region specialized for the perception of faces.

TMS evidence for the involvement of the right occipital face area in early face processing.

What's in a face? Effects of stimulus duration and inversion on face processing in schizophrenia.

The validity of the face-selective ERP N170 component during simultaneous recording with functional MRI.

The asymmetry of the fusiform face area is a stable individual characteristic that underlies the left-visual-field superiority for faces.

The representations of spacing and part-based information are associated for upright faces but dissociated for objects: evidence from individual differences.

No global processing deficit in the Navon task in 14 developmental prosopagnosics.

Diminished neural sensitivity to irregular facial expression in first-episode schizophrenia.

The role of skin colour in face recognition.

The shape of facial features and the spacing among them generate similar inversion effects: a reply to Rossion (2008).

Why does picture-plane inversion sometimes dissociate perception of features and spacing in faces, and sometimes not? Toward a new theory of holistic processing.

Diagnosing prosopagnosia: effects of ageing, sex, and participant-stimulus ethnic match on the Cambridge Face Memory Test and Cambridge Face Perception Test.

Event-related potential and functional MRI measures of face-selectivity are highly correlated: a simultaneous ERP-fMRI investigation.

External facial features modify the representation of internal facial features in the fusiform face area.

Nonpreferred stimuli modify the representation of faces in the fusiform face area.

It's all in your head: why is the body inversion effect abolished for headless bodies?

Why is the N170 enhanced for inverted faces? An ERP competition experiment.

The body inversion effect is mediated by face-selective, not body-selective, mechanisms.

Prosopagnosia as an impairment to face-specific mechanisms: Elimination of the alternative hypotheses in a developmental case.

Rapid object category adaptation during unlabelled classification.

The structure of face--space is tolerant to lighting and viewpoint transformations.

The role of lateral occipital face and object areas in the face inversion effect.

Stimulation of category-selective brain areas modulates ERP to their preferred categories.

Face ethnicity and measurement reliability affect face recognition performance in developmental prosopagnosia: evidence from the Cambridge Face Memory Test-Australian.

Can massive but passive exposure to faces contribute to face recognition abilities?

Start position strongly influences fixation patterns during face processing: difficulties with eye movements as a measure of information use.

Hierarchical processing of face viewpoint in human visual cortex.

Let's face it, from trial to trial: comparing procedures for N170 single-trial estimation.

Do object-category selective regions in the ventral visual stream represent perceived distance information?

A face inversion effect without a face.

A robust method of measuring other-race and other-ethnicity effects: the Cambridge Face Memory Test format.

Face recognition systems in monkey and human: are they the same thing?

A unified coding strategy for processing faces and voices.

The challenge of localizing the anterior temporal face area: a possible solution.

Face perception is category-specific: evidence from normal body perception in acquired prosopagnosia.

Separate parts of occipito-temporal white matter fibers are associated with recognition of faces and places.

Clutter modulates the representation of target objects in the human occipitotemporal cortex.

Neural Correlates of Subliminal Language Processing.

An Integrated Face-Body Representation in the Fusiform Gyrus but Not the Lateral Occipital Cortex.