Kristen West

发表

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

Christian Gieger, Thomas Meitinger, Chao-Yu Guo, 2006, Nature Genetics.

Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.

E. Grice, A. McCallion, A. Chakravarti, 2010, American journal of human genetics.

Widespread microRNA repression by Myc contributes to tumorigenesis

Tsung-Cheng Chang, E. Wentzel, D. Arking, 2008, Nature Genetics.

A resource for analysis of microRNA expression and function in pancreatic ductal adenocarcinoma cells

O. Kent, M. Mullendore, D. Arking, 2009, Cancer biology & therapy.

Hirschsprung disease, associated syndromes and genetics: a review

A Chakravarti, G Burzynski, Erasmus Mc, 2001, Journal of Medical Genetics.

Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability.

Jeffrey J. Gray, Albee Y. Ling, Seneca L. Bessling, 2015, American journal of human genetics.

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Tanya M. Teslovich, E. Cook, A. Chakravarti, 2008, American journal of human genetics.

Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.

A. Chakravarti, D. Cutler, D. Arking, 2006, Gastroenterology.

Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.

Christine A Iacobuzio-Donahue, Aravinda Chakravarti, Scott E Kern, 2006, Cancer research.