David J Cutler PhD

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Works 1-10 of 45

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Article

Susceptibility to childhood onset rheumatoid arthritis: Investigation of a weighted genetic risk score that integrates cumulative effects of variants at five genetic loci

by Sampath Prahalad; Karen N Conneely; Yunxuan Jiang; Marc Sudman; Carol A. Wallace; Milton R Brown; Lori A. Ponder; Mina Rohani-Pichavant; Michael Zwick; David J Cutler; Sheila Angeles-Han; Larry B Vogler; Christine Kennedy; Kelly A. Rouster Stevens; Carol A. Wise; Marilynn Punaro; Ann M. Reed; Elizabeth D. Mellins; John F. Bohnsack; David N. Glass; Susan D. Thompson

2013

Article

Recessive gene disruptions in autism spectrum disorder

by David Cutler; RN Doan; ET Lim; S De Rubeis; C Betancur; AG Chiocchetti; LM Overman; A Soucy; S Goetze; CM Freitag; MJ Daly; CA Walsh; JD Buxbaum; TW Yu

2019

Article

Targeted Sequencing of the Human X Chromosome Exome

by Kajari Mondal; Amol Carl Shetty; Viren Patel; David J Cutler; Michael Zwick

2011

Article

Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping.

by David J Cutler; Michael Zwick; David T. Okou; Sampath Prahalad; Thomas Walters; Stephen L. Guthery; Marla Dubinsky; Robert Baldassano; Wallace V. Crandall; Joel Rosh ; James Markowitz; Michael Stephens; Richard Kellermayer; Marian Pfefferkon; Melvin B. Heyman; Neal LeLeiko; David Mack; Dedrick Moulton; Michael D. Kappelman; Archana Kumar; Jarod Prince; Promita Bose; Kajari Mondal; Dhanya Ramchandran; John F. Bohnsack; Anne M. Griffiths ; Yael Haberman; Jonah Essers; Susan D. Thompson; Bruce Aronow; David J. Keljo; Jeffrey S. Hyams; Lee A. Denson; Subra Kugathasan

2015

Article

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

by Jack A. Kosmicki; Kaitlin E. Samocha; Daniel P. Howrigan; Stephan J. Sanders; Kamil Slowikowski; Monkol Lek; Konrad J. Karczewski; David Cutler; Bernie Devlin; Kathryn Roeder; Joseph D. Buxbaum; Benjamin M. Neale; Daniel G. MacArthur; Dennis P. Wall; Elise B. Robinson; Mark J. Daly

2017

Article

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

by Jennifer Mulle; Ann E. Pulver; John M. McGrath; Paula Wolyniec; Anne F. Dodd; David Cutler; Jonathan Sebat; Dheeraj Malhotra; Gerald Nestadt; Donald F. Conrad; Matthew Hurles; Chris P. Barnes; Masashi Ikeda; Nakao Iwata; Douglas F. Levinson; Pablo V. Gejman; Alan R. Sanders; Jubao Duan; Adele A. Mitchell; Inga Peter; Pamela Sklar; Colm T. O'Dushlaine; Detelina Grozeva; Michael C. O'Donovan; Michael J. Owen; Christina M. Hultman; Anna K. Kahler; Patrick F. Sullivan; George Kirov; Stephen Warren

2014

Article

Genome-wide association study of down syndrome-associated atrioventricular septal defects

by Dhanya Ramachandran; Zhen Zeng; Adam E. Locke; Jennifer Mulle; Lora Bean; Tracie Rosser; Kenneth Dooley; Clifford L. Cua; George T. Capone; Roger H. Reeves; Cheryl L. Maslen; David Cutler; Eleanor Feingold; Stephanie Sherman; Michael Zwick

2015