[PDF][PDF] Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

…, P Kohn, CB Mervis, JS Kippenhan… - Neuron, 2004 - cell.com
A unique opportunity to understand genetic determinants of cognition is offered by Williams
syndrome (WS), a well-characterized hemideletion on chromosome 7q11.23 that causes …

Genetic contributions to human gyrification: sulcal morphometry in Williams syndrome

JS Kippenhan, RK Olsen, CB Mervis… - Journal of …, 2005 - Soc Neuroscience
Although gyral and sulcal patterns are highly heritable, and emerge in a tightly controlled
sequence during development, very little is known about specific genetic contributions to …

[PDF][PDF] Regional variations in brain gyrification are associated with general cognitive ability in humans

MD Gregory, JS Kippenhan, D Dickinson, J Carrasco… - Current Biology, 2016 - cell.com
Searching for a neurobiological understanding of human intellectual capabilities has long
occupied those very capabilities. Brain gyrification, or folding of the cortex, is as highly evolved …

[HTML][HTML] Neanderthal-derived genetic variation shapes modern human cranium and brain

MD Gregory, JS Kippenhan, DP Eisenberg, PD Kohn… - Scientific reports, 2017 - nature.com
Before their disappearance from the fossil record approximately 40,000 years ago, Neanderthals,
the ancient hominin lineage most closely related to modern humans, interbred with …

Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome

S Marenco, MA Siuta, JS Kippenhan… - Proceedings of the …, 2007 - National Acad Sciences
Little is known about genetic regulation of the development of white matter. This knowledge
is critical in understanding the pathophysiology of neurodevelopmental syndromes …

Reading, hearing, and the planum temporale

…, RK Olsen, PF Koch, P Kohn, JS Kippenhan… - Neuroimage, 2005 - Elsevier
Many neuroimaging studies of single-word reading have been carried out over the last 15
years, and a consensus as to the brain regions relevant to this task has emerged. Surprisingly, …

The Williams syndrome chromosome 7q11. 23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function

M Jabbi, JS Kippenhan, P Kohn… - Proceedings of the …, 2012 - National Acad Sciences
Although it is widely accepted that genes can influence complex behavioral traits such as
human temperament, the underlying neurogenetic mechanisms remain unclear. Williams …

Transport of platelets in flowing blood.

…, DL Bilsker, CM Waters, JS Kippenhan… - Annals of the New …, 1987 - europepmc.org
Distribution and transport of platelets in flowing blood were studied experimentally using
suspensions of washed red cells and fluorescent latex beads as platelet analogues. …

Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis

…, M Hamborg, JS Kippenhan… - American Journal of …, 2021 - Wiley Online Library
Schizophrenia has been hypothesized to be a human‐specific condition, but experimental
approaches to testing this idea have been limited. Because Neanderthals, our closest …

Convergent BOLD and beta-band activity in superior temporal sulcus and frontolimbic circuitry underpins human emotion cognition

…, FW Carver, Q Chen, B Cropp, JS Kippenhan… - Cerebral …, 2015 - academic.oup.com
The processing of social information in the human brain is widely distributed neuroanatomically
and finely orchestrated over time. However, a detailed account of the spatiotemporal …