Literature DB >> 20488247

V1 is not uniquely identified by polarity reversals of responses to upper and lower visual field stimuli.

Justin M Ales1, Jacob L Yates, Anthony M Norcia.   

Abstract

The cruciform hypothesis states that if a visual evoked potential component originates in V1, then stimuli placed in the upper versus lower visual fields will generate responses with opposite polarity at the scalp. This diagnostic has been used by many studies as a definitive marker of V1 sources. To provide an empirical test of the validity of the cruciform hypothesis, we generated forward models of cortical areas V1, V2 and V3 that were based on realistic estimates of the 3-D shape of these areas and the shape and conductivity of the brain, skull and scalp. Functional MRI was used to identify the location of early visual areas and anatomical MRI data was used to construct detailed cortical surface reconstructions and to generate boundary element method forward models of the electrical conductivity of each participant's head. These two data sets for each subject were used to generate simulated scalp activity from the dorsal and ventral subdivisions of each visual area that correspond to the lower and upper visual field representations, respectively. The predicted topographies show that sources in V1 do not fully conform to the cruciform sign-reversal. Moreover, contrary to the model, retinotopic visual areas V2 and V3 show polarity reversals for upper and lower field stimuli. The presence of a response polarity inversion for upper versus lower field stimuli is therefore an insufficient criterion for identifying responses as having originated in V1. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20488247      PMCID: PMC2922686          DOI: 10.1016/j.neuroimage.2010.05.016

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  30 in total

1.  Using multi-stimulus VEP source localization to obtain a retinotopic map of human primary visual cortex.

Authors:  S D Slotnick; S A Klein; T Carney; E Sutter; S Dastmalchi
Journal:  Clin Neurophysiol       Date:  1999-10       Impact factor: 3.708

2.  Cortical sources of the early components of the visual evoked potential.

Authors:  Francesco Di Russo; Antígona Martínez; Martin I Sereno; Sabrina Pitzalis; Steven A Hillyard
Journal:  Hum Brain Mapp       Date:  2002-02       Impact factor: 5.038

3.  Study of the visual evoked magnetic field with the m-sequence technique.

Authors:  Hitoshi Tabuchi; Tsuranu Yokoyama; Masahiro Shimogawara; Kunihiko Shiraki; Eiichiro Nagasaka; Tokuhiko Miki
Journal:  Invest Ophthalmol Vis Sci       Date:  2002-06       Impact factor: 4.799

4.  Consistent and precise localization of brain activity in human primary visual cortex by MEG and fMRI.

Authors:  F Moradi; L C Liu; K Cheng; R A Waggoner; K Tanaka; A A Ioannides
Journal:  Neuroimage       Date:  2003-03       Impact factor: 6.556

5.  The pattern-pulse multifocal visual evoked potential.

Authors:  Andrew Charles James
Journal:  Invest Ophthalmol Vis Sci       Date:  2003-02       Impact factor: 4.799

6.  A principal component analysis of multifocal pattern reversal VEP.

Authors:  Xian Zhang; Donald C Hood
Journal:  J Vis       Date:  2004-02-04       Impact factor: 2.240

7.  Flow of activation from V1 to frontal cortex in humans. A framework for defining "early" visual processing.

Authors:  John J Foxe; Gregory V Simpson
Journal:  Exp Brain Res       Date:  2001-11-15       Impact factor: 1.972

8.  The folding fingerprint of visual cortex reveals the timing of human V1 and V2.

Authors:  Justin Ales; Thom Carney; Stanley A Klein
Journal:  Neuroimage       Date:  2009-09-22       Impact factor: 6.556

9.  Functional measurements of human ventral occipital cortex: retinotopy and colour.

Authors:  Alex R Wade; Alyssa A Brewer; Jochem W Rieger; Brian A Wandell
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-08-29       Impact factor: 6.237

Review 10.  Fast robust automated brain extraction.

Authors:  Stephen M Smith
Journal:  Hum Brain Mapp       Date:  2002-11       Impact factor: 5.038

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  34 in total

1.  Isolating early cortical generators of visual-evoked activity: a systems identification approach.

Authors:  Jeremy W Murphy; Simon P Kelly; John J Foxe; Edmund C Lalor
Journal:  Exp Brain Res       Date:  2012-05-29       Impact factor: 1.972

2.  The cruciform model of striate generation of the early VEP, re-illustrated, not revoked: a reply to Ales et al. (2013).

Authors:  Simon P Kelly; M Isabel Vanegas; Charles E Schroeder; Edmund C Lalor
Journal:  Neuroimage       Date:  2013-06-02       Impact factor: 6.556

3.  Visual field asymmetries in visual evoked responses.

Authors:  Donald J Hagler
Journal:  J Vis       Date:  2014-12-19       Impact factor: 2.240

4.  Effects of Stimulus Size and Contrast on the Initial Primary Visual Cortical Response in Humans.

Authors:  Nigel Gebodh; M Isabel Vanegas; Simon P Kelly
Journal:  Brain Topogr       Date:  2017-05-04       Impact factor: 3.020

5.  Earliest stages of visual cortical processing are not modified by attentional load.

Authors:  Yulong Ding; Antigona Martinez; Zhe Qu; Steven A Hillyard
Journal:  Hum Brain Mapp       Date:  2013-11-04       Impact factor: 5.038

6.  Modulation of early cortical processing during divided attention to non-contiguous locations.

Authors:  Hans-Peter Frey; Anita M Schmid; Jeremy W Murphy; Sophie Molholm; Edmund C Lalor; John J Foxe
Journal:  Eur J Neurosci       Date:  2014-03-07       Impact factor: 3.386

7.  Detailed spatiotemporal brain mapping of chromatic vision combining high-resolution VEP with fMRI and retinotopy.

Authors:  Sabrina Pitzalis; Francesca Strappini; Alessandro Bultrini; Francesco Di Russo
Journal:  Hum Brain Mapp       Date:  2018-03-13       Impact factor: 5.038

8.  The inferior occipital gyrus is a major cortical source of the face-evoked N170: Evidence from simultaneous scalp and intracerebral human recordings.

Authors:  Corentin Jacques; Jacques Jonas; Louis Maillard; Sophie Colnat-Coulbois; Laurent Koessler; Bruno Rossion
Journal:  Hum Brain Mapp       Date:  2018-11-12       Impact factor: 5.038

9.  Human Sensory Cortex Contributes to the Long-Term Storage of Aversive Conditioning.

Authors:  Yuqi You; Joshua Brown; Wen Li
Journal:  J Neurosci       Date:  2021-02-23       Impact factor: 6.167

10.  Contrast Normalization Accounts for Binocular Interactions in Human Striate and Extra-striate Visual Cortex.

Authors:  Chuan Hou; Spero C Nicholas; Preeti Verghese
Journal:  J Neurosci       Date:  2020-02-14       Impact factor: 6.167

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