Retinotopy and Functional Subdivision of Human Areas MT and MST
By Alexander C. Huk, Robert F. Dougherty, David J. Heeger. Journal of Neuroscience, 2002
656 citations recorded by the source corpus.
Subfields: Cognitive Neuroscience, Molecular Biology, Neurology
View Paper: https://www.semanticscholar.org/paper/39a569a24b613df7183d0cce94493634b5dce0df
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cognitive Neuroscience
- Matthew F. Glasser
- D. V. Van Essen
- Timothy S. Coalson
- B. T. T. Yeo
- Randy L. Buckner
- Mert Rory Sabuncu
- Donna L. Dierker
- Fenna M. Krienen
In Molecular Biology
- Jonathan Winawer
- D. V. Van Essen
- Alvaro Pascual-Leone
- B. T. T. Yeo
- Bruce Fischl
- Jordan W. Smoller
- Brian A. Wandell
- Matthew F. Glasser
In Neurology
- Guy A. Orban
- Wim Vanduffel
- Alvaro Pascual-Leone
- Bruce Fischl
- Brian A. Wandell
- Matthew F. Glasser
- Jonathan Winawer
- Fenna M. Krienen
Citations in the corpus
- Using high-resolution quantitative mapping of R1 as an index of cortical myelination (2014, neutral): “…as MT/V5 in a number of studies, our retinotopicmapping data – including both polar anglemapping aswell as the location of the posterior boundary of ipsilateral responses in a localizer task (Huk et al., 2002) – showed that MT proper only accounted for the posterior 1/3 to 1/2 of that oval.”
- Imaging retinotopic maps in the human brain (2010, methodology): “As methods developed and MR scanner technology advanced , it became possible to identify retinotopic organization in MT+, and several groups now report that the region appears to have at least two visual field maps (Amano et al., 2009; Dukelow et al., 2001; Georgieva et al., 2009; Huk et al., 2002).”
- Mapping Human Cortical Areas in vivo Based on Myelin Content as Revealed by T1- and T2-weighted MRI (2011, background): “This difference suggests that the heavily myelinated region includes other heavily myelinated portions of the MT complex, perhaps including middle superior temporal area (MST) and floor of superior temporal area (FST) (Huk et al., 2002; Kolster et al., 2010).”
- Visual field maps in human cortex. (2007, neutral): “…early studies of human visual field maps use nomenclature established in nonhuman primate studies, i.e., Vx (DeYoe et al., 1996; Dumoulin et al., 2000; Engel et al., 1997; Huk et al., 2002; Schneider et al., 1993; Sereno et al., 1995; Tootell et al., 1995; Watson et al., 1993; Zeki et al., 1991).”
- Motion-dependent representation of space in area MT+ (2013, neutral): “Area MT in the macaque monkey, and its human homolog hMT+, has been shown to represent positions coarsely in a retinotopic manner (Gattass and Gross, 1981; Huk et al., 2002; Wandell et al., 2007).”
- Comparative mapping of higher visual areas in monkeys and humans. (2004, background): “Nonetheless there is widespread consensus that its more posterior portion is a homologue of macaque MT [ 35 ].”
- Human Neuroscience (neutral): “…on the STS that are invariant to changes size perspective (Jellema et al., 2004), and extend them to related cortical areas. hemifi eld representations (such as in hMT, Huk et al., 2002), the shifted position trials were analyzed relative to the hemisphere, as Contralateral or Ipsilateral shifts.”
- Charting the Lower Superior Temporal Region, a New Motion-Sensitive Region in Monkey Superior Temporal Sulcus (2006, background): “In humans, attempts have been made to parcel the human MT/V5 complex (Dukelow et al., 2001; Huk et al., 2002), but these have been restricted to identifying the homolog of the MST area.”
- The organization of the human cerebral cortex estimated by intrinsic functional connectivity. (2011, background): “1995) and motion-selective area MT (Huk et al. 2002; Malikovic et al. 2007; Tootell and Taylor 1995).”
- Parcellations and hemispheric asymmetries of human cerebral cortex analyzed on surface-based atlases. (2012, methodology): “However, motion-selective fMRI activations extend across multiple cortical areas in lateral occipitotemporal cortex (Tootell et al. 1995; Huk et al. 2002; Figure 12.”
- Alpha-beta and gamma rhythms subserve feedback and feedforward influences among human visual cortical areas (2016, neutral): “In the human brain, area MT has been consistently mapped at a corresponding location, has a similar visuotopic organization and is characterized by its motion-selective activation (Huk et al., 2002; Fischl et al., 2008; Kolster et al., 2010).”
- Repetitive TMS over posterior STS disrupts perception of biological motion. (2005, background): “Human MT+/V5 receives input corresponding to a contralateral visual field representation (Huk et al., 2002), while the cortical organization of pSTS is thought to include the full visual field (Grossman et al., 2000).”