The Contribution of Mosaic Variants to Autism Spectrum Disorder

per Freed, Donald, Pevsner, Jonathan
Publicat a PLoS Genet (2016)

Visualization of Shared Genomic Regions and Meiotic Recombination in High-Density SNP Data

per Roberson, Elisha D. O., Pevsner, Jonathan
Publicat 2009

The biology of the mammalian Krüppel-like family of transcription factors

per Dang, Duyen T., Pevsner, Jonathan, Yang, Vincent W.
Publicat 2000

Somatic Mosaicism in the Human Genome

per Freed, Donald, Stevens, Eric L., Pevsner, Jonathan
Publicat a Genes (Basel) (2014)

Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays

per Scharpf, Robert B., Parmigiani, Giovanni, Pevsner, Jonathan, Ruczinski, Ingo
Publicat 2008

Locations and patterns of meiotic recombination in two-generation pedigrees

per Ting, Jason C, Roberson, Elisha DO, Currier, Duane G, Pevsner, Jonathan
Publicat 2009

Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method

per Baugher, Joseph D, Baugher, Benjamin D, Shirley, Matthew D, Pevsner, Jonathan
Publicat 2013

Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan

per Thomas George H, Ye Ying, Ting Jason C, Ruczinski Ingo, Pevsner Jonathan
Publicat 2006-01-01

Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan

per Ting, Jason C, Ye, Ying, Thomas, George H, Ruczinski, Ingo, Pevsner, Jonathan
Publicat 2006

Syntaxin 7 and VAMP-7 are Soluble N-Ethylmaleimide–sensitive Factor Attachment Protein Receptors Required for Late Endosome–Lysosome and Homotypic Lysosome Fusion in Alveolar Macro...

per Ward, Diane McVey, Pevsner, Jonathan, Scullion, Matthew A., Vaughn, Michael, Kaplan, Jerry
Publicat 2000

Efficient Array-Based Identification of Novel Cardiac Genes through Differentiation of Mouse ESCs

per Miller, Ronald A., Christoforou, Nicolas, Pevsner, Jonathan, McCallion, Andrew S., Gearhart, John D.
Publicat 2008

Altered Patterns of Cellular Gene Expression in Dermal Microvascular Endothelial Cells Infected with Kaposi's Sarcoma-Associated Herpesvirus

per Poole, Lynn J., Yu, Yanxing, Kim, Peter S., Zheng, Qi-Zhi, Pevsner, Jonathan, Hayward, Gary S.
Publicat 2002

Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models

per Wang, Wenyi, Carvalho, Benilton, Miller, Nathaniel D., Pevsner, Jonathan, Chakravarti, Aravinda, Irizarry, Rafael A.
Publicat 2008

Unexpected Relationships and Inbreeding in HapMap Phase III Populations

per Stevens, Eric L., Baugher, Joseph D., Shirley, Matthew D., Frelin, Laurence P., Pevsner, Jonathan
Publicat 2012

Genetic and genomic stability across lymphoblastoid cell line expansions

per Scheinfeldt, Laura B., Hodges, Kelly, Pevsner, Jonathan, Berlin, Dorit, Turan, Nahid, Gerry, Norman P.
Publicat a BMC Res Notes (2018)

Consanguinity in Centre d'Étude du Polymorphisme Humain (CEPH) pedigrees

per Stevens, Eric L, Heckenberg, Greg, Baugher, Joseph D, Roberson, Elisha DO, Downey, Thomas J, Pevsner, Jonathan
Publicat 2012

Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State

per Stevens, Eric L., Heckenberg, Greg, Roberson, Elisha D. O., Baugher, Joseph D., Downey, Thomas J., Pevsner, Jonathan
Publicat 2011

A Novel Variantin GABRB2 Associated with Intellectual Disability and Epilepsy

per Srivastava, Siddharth, Cohen, Julie, Pevsner, Jonathan, Aradhya, Swaroop, McKnight, Dianalee, Butler, Elizabeth, Johnston, Michael, Fatemi, Ali
Publicat 2014

Molecular (SNP) Analyses of Overlapping Hemizygous Deletions of 10q25.3 to 10qter in Four Patients: Evidence for HMX2 and HMX3 as Candidate Genes in Hearing and Vestibular Function

per Miller, Nathaniel D., Nance, Melonie A., Wohler, Elizabeth S., Hoover-Fong, Julie E., Lisi, Emily, Thomas, George H., Pevsner, Jonathan
Publicat 2009

Chromosomal variation in lymphoblastoid cell lines

per Shirley, Matthew D., Baugher, Joseph D., Stevens, Eric L., Tang, Zhenya, Gerry, Norman, Beiswanger, Christine M., Berlin, Dorit S., Pevsner, Jonathan
Publicat 2012