Ravinesh A. Kumar

发表

Microduplications of 16p11.2 are Associated with Schizophrenia

Jessica R. Wolff, J. Sebat, B. Lakshmi, 2009, Nature Genetics.

Recurrent 16p11.2 microdeletions in autism.

D. Conrad, T. Gilliam, Ravinesh A. Kumar, 2007, Human molecular genetics.

Selected summaries from the XVI World Congress of Psychiatric Genetics, Osaka, Japan, 11–15 October 2008

Ravinesh A. Kumar, L. DeLisi, L. M. Houlihan, 2009, Psychiatric genetics.

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

Ravinesh A. Kumar, S. Christian, E. Cook, 2008, Biological Psychiatry.

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function

J. Rosenfeld, W. Chung, L. Shaffer, 2011, European Journal of Human Genetics.

Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

S. Scherer, J. Sutcliffe, D. Geschwind, 2009, PloS one.

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

Ravinesh A. Kumar, S. Christian, E. Cook, 2009, Journal of Medical Genetics.

Of Mice and Men

Ravinesh A. Kumar, E. Simpson, T. Nicholls, 2005, Journal of interpersonal violence.

Genetics of autism spectrum disorders

Ravinesh A. Kumar, S. Christian, Susan L Christian, 2009, Current neurology and neuroscience reports.

Duplication 16p11.2 in a child with infantile seizure disorder

Ravinesh A. Kumar, S. Christian, D. M. Martin, 2010, American journal of medical genetics. Part A.

Unexpected embryonic stem (ES) cell mutations represent a concern in gene targeting: Lessons from “fierce” mice

Ravinesh A. Kumar, B. Abrahams, E. Simpson, 2004, Genesis.

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

Ravinesh A. Kumar, M. Topf, D. Pilz, 2010, Human molecular genetics.

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles

H. Peeters, J. Sebat, D. Malhotra, 2015, Journal of child neurology.

Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing

Ravinesh A. Kumar, B. Abrahams, E. Simpson, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Copy number and sequence variants implicate APBA2 as an autism candidate gene

Ravinesh A. Kumar, S. Christian, W. Dobyns, 2009, Autism research : official journal of the International Society for Autism Research.

Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

C. T. Morgan, Ravinesh A. Kumar, E. Simpson, 2007, BMC Medical Genetics.

Duplication 16p11.2 in a child with infantile seizure disorder

Ravinesh A. Kumar, S. Christian, D. M. Martin, 2010, American journal of medical genetics. Part A.