Jeffrey C. Murray

发表

Detection of de novo copy number deletions from targeted sequencing of trios

Mary L. Marazita, Ingo Ruczinski, Jack M. Fu, 2018 .

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives

Ingo Ruczinski, Alexandre Bureau, Hasan Albacha-Hejazi, 2014, Bioinform..

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Mary L. Marazita, Ingo Ruczinski, Ferdouse Begum, 2018 .

Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability

Jeffrey C. Murray, Robert E. Malone, Heidi Major Sleister, 1992, Nucleic Acids Res..

Detection of de novo copy number deletions from targeted sequencing of trios

Ingo Ruczinski, Jack M. Fu, Elizabeth J. Leslie, 2018, bioRxiv.

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Ingo Ruczinski, Li-e Wang, William L. Lowe, 2012, Nature Genetics.

The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community

Seth M. Weinberg, Chung How Kau, Michael L. Cunningham, 2016, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Jeffrey C. Murray, Michael J. Dixon, Andrew C. Lidral, 2002, Nature Genetics.

Evidence for gene-environment interaction in a genome wide study of isolated, non-syndromic cleft palate

Holger Schwender, Ingo Ruczinski, Alan F. Scott, 2011 .

A Mutation in Mouse Pak1ip1 Causes Orofacial Clefting while Human PAK1IP1 Maps to 6p24 Translocation Breaking Points Associated with Orofacial Clefting

Youngshik Choe, Jeffrey C. Murray, Richard Sturm, 2013, PloS one.

Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice

Jeffrey C. Murray, Stuart Schwartz, Clemencia Colmenares, 2002, Nature Genetics.

The Stored Tissue Issue: Biomedical Research, Ethics, and Law in the Era of Genomic Medicine

Robert F. Weir, Jeffrey C. Murray, R. Weir, 2004 .

Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease

Naoyuki Taniguchi, Jeffrey C. Murray, Kunihiro Yoshida, 2000, Nature Genetics.

Disruption of an AP-2α binding site in an IRF6 enhancer is strongly associated with cleft lip

Axel Visel, Len A. Pennacchio, Jeffrey C. Murray, 2008, Nature Genetics.

Noninvasive Whole-Genome Sequencing of a Human Fetus

Jay Shendure, Matthew W. Snyder, Jeffrey C. Murray, 2012, Science Translational Medicine.