Aravinda Chakravarti

发表

Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples.

P. Patel, A. Chakravarti, A. Sanders, 1996, American journal of medical genetics.

No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families

A. Chakravarti, J. Mulle, V. Nimgaonkar, 2005, Molecular Psychiatry.

Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.

S. Schwartz, A. Chakravarti, S. Bolk, 1996, American journal of medical genetics.

The Fate of 12 Recessive Mutations in A Single Village

A. Chakravarti, J. Zlotogora, S. Shalev, 2007, Annals of human genetics.

Inheritance pattern of platelet membrane fluidity in Alzheimer disease.

A. Chakravarti, S. Slaugenhaupt, G. Zubenko, 1989, American journal of human genetics.

Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.

U. Surti, A. Chakravarti, R. Ferrell, 1990, American journal of human genetics.

Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene.

H. Hong, J. Lass, A. Chakravarti, 1999, Human molecular genetics.

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

D. Ledbetter, S. Malcolm, M. Butler, 1993, Human molecular genetics.

Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.

U. Surti, A. Chakravarti, T. Hassold, 2000, American journal of human genetics.

Cardiac muscle–restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features

A. Kapoor, D. Auer, Alexa Smith, 2023, G3.

Multipoint gene mapping using seriation. I. General methods.

K H Buetow, A Chakravarti, K. Buetow, 1987, American journal of human genetics.