FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Adria Bodell

Research Profile

Concepts & Ideas

Physiology

Disorders

Anatomy

Co-author Network

Publications

TOP 3
Ganeshwaran H Mochida; Muhammad Mahajnah; Anthony D Hill; Lina Basel-Vanagaite; Danielle Gleason; R Sean Hill; Adria Bodell; Moira Crosier; Rachel Straussberg; Christopher Walsh
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.
Eric M Morrow; Seung-Yun Yoo; Steven W Flavell; Tae-kyung Kim; Yingxi Lin; Robert Sean Hill; Nahit M Mukaddes; Soher Balkhy; Generoso Gascon; Asif Hashmi; Samira Al-Saad; Janice Ware; Robert M Joseph; Rachel Greenblatt; Danielle Gleason; Julia A Ertelt; Kira A Apse; Adria Bodell; Jennifer N Partlow; Brenda Barry; Hui Yao; Kyriacos Markianos; Russell J Ferland; Michael E Greenberg; Christopher Walsh
Identifying autism loci and genes by tracing recent shared ancestry.
Bernard S Chang; T Katzir; Tianming Liu; K Corriveau; M Barzillai; Kira Apse; Adria Bodell; D Hackney; David Alsop; Stephen Wong; S Wong; Christopher Walsh
A structural basis for reading fluency: white matter defects in a genetic brain malformation.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Adria Bodell (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2009: Ganeshwaran H Mochida; Muhammad Mahajnah; Anthony D Hill; Lina Basel-Vanagaite; Danielle Gleason; R Sean Hill; Adria Bodell; Moira Crosier; Rachel Straussberg; Christopher Walsh
A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.
American journal of human genetics 2009;85(6):897-902.
2008: Eric M Morrow; Seung-Yun Yoo; Steven W Flavell; Tae-kyung Kim; Yingxi Lin; Robert Sean Hill; Nahit M Mukaddes; Soher Balkhy; Generoso Gascon; Asif Hashmi; Samira Al-Saad; Janice Ware; Robert M Joseph; Rachel Greenblatt; Danielle Gleason; Julia A Ertelt; Kira A Apse; Adria Bodell; Jennifer N Partlow; Brenda Barry; Hui Yao; Kyriacos Markianos; Russell J Ferland; Michael E Greenberg; Christopher Walsh
Identifying autism loci and genes by tracing recent shared ancestry.
Science (New York, N.Y.) 2008;321(5886):218-23.
2007: Bernard S Chang; T Katzir; Tianming Liu; K Corriveau; M Barzillai; Kira Apse; Adria Bodell; D Hackney; David Alsop; Stephen Wong; S Wong; Christopher Walsh
A structural basis for reading fluency: white matter defects in a genetic brain malformation.
Neurology 2007;69(23):2146-54.
2007: Anthony Hill; Bernard S Chang; R Sean Hill; Levi A Garraway; Adria Bodell; William R Sellers; Christopher Walsh
A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome.
American journal of medical genetics. Part A 2007;143A(15):1692-8.
2007: Ian Tietjen; Adria Bodell; Kira Apse; Ashley M Mendonza; Bernard S Chang; Gary M Shaw; A James Barkovich; Edward J Lammer; Christopher Walsh
Comprehensive EMX2 genotyping of a large schizencephaly case series.
American journal of medical genetics. Part A 2007;143A(12):1313-6.
2006: Jason Neal; Praveen B Raju; Adria Bodell; Kira Apse; Christopher Walsh; Volney L Sheen
Periventricular heterotopia with complete agenesis of the corpus callosum : a case report.
Journal of neurology 2006;253(10):1358-9.
2006: Anna Rajab; Seung-Yun Yoo; Aiman Abdulgalil; Salem Kathiri; Riaz Ahmed; Ganeshwaran H Mochida; Adria Bodell; A James Barkovich; Christopher Walsh
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.
American journal of medical genetics. Part A 2006;140(14):1504-10.
2006: Marcelo R Masruha; Luís Otávio Sales Ferreira Caboclo; Henrique Carrete; Iscia L Cendes; Murilo G Rodrigues; Eliana Garzon; Elza Márcia Targas Yacubian; Américo C Sakamoto; Volney L Sheen; Megan Harney; Jason Neal; R Sean Hill; Adria Bodell; Christopher Walsh; Luiz Celso Pereira Vilanova
Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males.
Epilepsia 2006;47(1):211-4.
2005: Xianhua Piao; Bernard S Chang; Adria Bodell; Katelyn Woods; Bruria Benzeev; Meral Topcu; Renzo Guerrini; Hadassa Goldberg-Stern; László Sztriha; William B Dobyns; A James Barkovich; Christopher Walsh
Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.
Annals of neurology 2005;58(5):680-7.
2005: J Shen; Wafaa Eyaid; Ganeshwaran H Mochida; F Al-Moayyad; Adria Bodell; C Geoffrey Woods; Christopher Walsh
ASPM mutations identified in patients with primary microcephaly and seizures.
Journal of medical genetics 2005;42(9):725-9.
2005: Bernard S Chang; J Ly; B Appignani; Adria Bodell; Kira Apse; R S Ravenscroft; Volney L Sheen; M J Doherty; D B Hackney; M O'Connor; A M Galaburda; Christopher Walsh
Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia.
Neurology 2005;64(5):799-803.
2005: Sophie C Currier; Christine K Lee; Bernard S Chang; Adria Bodell; G Shashidhar Pai; Leela Job; Lieven Lagae; Lihadh Al-Gazali; Wafaa Eyaid; Greg Enns; William B Dobyns; Christopher Walsh
Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome.
American journal of medical genetics. Part A 2005;133A(1):53-7.
2004: Russell J Ferland; Wafaa Eyaid; Randall V Collura; Laura D Tully; R Sean Hill; Doha Al-Nouri; Ahmed Al-Rumayyan; Meral Topcu; Generoso Gascon; Adria Bodell; Yin Yao Shugart; Maryellen Ruvolo; Christopher Walsh
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.
Nature genetics 2004;36(9):1008-13.
2004: Volney L Sheen; Lina Basel-Vanagaite; Jean R Goodman; Ingrid E Scheffer; Adria Bodell; Vijay S Ganesh; Robert Ravenscroft; R Sean Hill; Timothy J Cherry; Yin Yao Shugart; James Barkovich; Rachel Straussberg; Christopher Walsh
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus.
Brain & development 2004;26(5):326-34.
2004: Ganeshwaran H Mochida; Anna Rajab; Wafaa Eyaid; A Lu; D Al-Nouri; Kenjiro Kosaki; mehrdad noruzinia; P Sarda; J Ishihara; Adria Bodell; Kira Apse; Christopher Walsh
Broader geographical spectrum of Cohen syndrome due to COH1 mutations.
Journal of medical genetics 2004;41(6):e87.
2004: Bernard S Chang; Xianhua Piao; C Giannini; G D Cascino; I Scheffer; C Geoffrey Woods; Meral Topcu; K Tezcan; Adria Bodell; R J Leventer; A James Barkovich; P Ellen Grant; Christopher Walsh
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation.
Neurology 2004;62(10):1722-8.
2004: Xianhua Piao; R Sean Hill; Adria Bodell; Bernard S Chang; Lina Basel-Vanagaite; Rachel Straussberg; William B Dobyns; Bassam Qasrawi; Robin M Winter; A Micheil Innes; Thomas Voit; M Elizabeth Ross; Jacques L Michaud; Jean-Claude Déscarie; A James Barkovich; Christopher Walsh
G protein-coupled receptor-dependent development of human frontal cortex.
Science (New York, N.Y.) 2004;303(5666):2033-6.
2004: Volney L Sheen; Vijay S Ganesh; Meral Topcu; Guillaume Sebire; Adria Bodell; R Sean Hill; P Ellen Grant; Yin Yao Shugart; Jaime Imitola; Samia J Khoury; Renzo Guerrini; Christopher Walsh
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.
Nature genetics 2004;36(1):69-76.
2003: Anna Rajab; Ganeshwaran H Mochida; Anthony Hill; Vijay S Ganesh; Adria Bodell; A Riaz; P Ellen Grant; Yin Yao Shugart; Christopher Walsh
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.
Neurology 2003;60(10):1664-7.
2003: Bernard S Chang; Xianhua Piao; Adria Bodell; Lina Basel-Vanagaite; Rachel Straussberg; William B Dobyns; Bassam Qasrawi; Robin M Winter; A Micheil Innes; Thomas Voit; P Ellen Grant; A James Barkovich; Christopher Walsh
Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.
Annals of neurology 2003;53(5):596-606.
2003: Volney L Sheen; Meral Topçu; SF Berkovic; Dilek Yalnizoglu; Ilan Blatt; Adria Bodell; R Sean Hill; Vijay S Ganesh; T J Cherry; Yin Yao Shugart; Christopher Walsh
Autosomal recessive form of periventricular heterotopia.
Neurology 2003;60(7):1108-12.
2003: Volney L Sheen; James W Wheless; Adria Bodell; E Braverman; Philip D Cotter; K A Rauen; O Glenn; Kara Weisiger; Seymour Packman; Christopher Walsh; Elliott H Sherr
Periventricular heterotopia associated with chromosome 5p anomalies.
Neurology 2003;60(6):1033-6.