E. Nickerson

发表

Genome sequencing in microfabricated high-density picolitre reactors

James R. Knight, J. W. Simpson, Bernard P. Puc, 2005, Nature.

Mutational heterogeneity in cancer and the search for new cancer-associated genes

Steven A. Roberts, T. Fennell, A. Sivachenko, 2013 .

Leigh syndrome transmitted by uniparental disomy of chromosome 9

L. Shaffer, E. Nickerson, WU MUILENBURGYUAN-QING, 1999 .

The generic genome browser: a building block for a model organism system database.

S. Lewis, L. Stein, M. Mangone, 2002, Genome research.

Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

Thomas LaFramboise, Levi A Garraway, Kwok-Kin Wong, 2006, Nature Medicine.

Mutational heterogeneity in cancer and the search for new cancer genes

Steven A. Roberts, David I Heiman, A. McKenna, 2014 .

A Landscape of Driver Mutations in Melanoma

A. Sivachenko, K. Cibulskis, S. Gabriel, 2012, Cell.

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

A. Sivachenko, K. Cibulskis, S. Gabriel, 2012, Nature Genetics.

Landscape of genomic alterations in cervical carcinomas

Trevor J Pugh, A. McKenna, K. Cibulskis, 2013, Nature.

Punctuated Evolution of Prostate Cancer Genomes

A. Sivachenko, K. Cibulskis, S. Gabriel, 2013, Cell.

A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence.

E. Nickerson, D. Nelson, S. Warren, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Melanoma genome sequencing reveals frequent PREX2 mutations

T. Fennell, A. Sivachenko, K. Cibulskis, 2012, Nature.

Genome Sequencing in Open Microfabricated High Density Picoliter Reactors

Yong Wang, Wen He, Joel S. Bader, 2005 .

Organism System Database The Generic Genome Browser: A Building Block for a Model

S. Lewis, L. Stein, M. Mangone, 2006 .

Leigh syndrome transmitted by uniparental disomy of chromosome 9

E. Nickerson, V. Tiranti, R. Marzella, 1999, Journal of medical genetics.

Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

L. Shaffer, E. Nickerson, M. Keating, 1995, American journal of human genetics.

Erratum: Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

J. Rothberg, J. Leamon, J. Simons, 2006, Nature Medicine.

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

L. Shaffer, J. Lupski, J. Korenberg, 1998, American journal of medical genetics.

Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.

S. Gabriel, E. Zackai, E. Nickerson, 2013, American journal of human genetics.

Exome sequencing of pleuropulmonary blastoma reveals frequent biallelic loss of TP53 and two hits in DICER1 resulting in retention of 5p-derived miRNA hairpin loop sequences

Trevor J Pugh, A. McKenna, K. Cibulskis, 2014, Oncogene.

Systematic genomic and translational efficiency studies of uveal melanoma

Ivana K. Kim, A. McKenna, K. Cibulskis, 2017, PloS one.

Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees.

E. Nickerson, D. Nelson, 1998, Genomics.

AMPD2 Regulates GTP Synthesis and Is Mutated in a Potentially Treatable Neurodegenerative Brainstem Disorder

S. Gabriel, E. Nickerson, R. Naviaux, 2013, Cell.

Detection of oncogenic mutations in the EGFR gene in lung adenocarcinoma with differential sensitivity to EGFR tyrosine kinase inhibitors.

J. Rothberg, J. Simons, M. Meyerson, 2005, Cold Spring Harbor symposia on quantitative biology.

Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders

Colin A. Johnson, S. Gabriel, E. Bertini, 2013, European Journal of Human Genetics.

Corrigendum: Genome sequencing in microfabricated high-density picolitre reactors

Yong Wang, Eugene W. Myers, Joel S. Bader, 2006, Nature.

Somatic mutation of CDKN1B in small intestine neuroendocrine tumors

Trevor J Pugh, J. Grimsby, N. Lennon, 2013, Nature Genetics.

Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome

S. Gabriel, E. Nickerson, J. Gleeson, 2012, Journal of Medical Genetics.

Deletions of the elastin gene in Williams Syndrome

E. Nickerson, F. Greenberg, C. McCaskill, 1994 .

Mutational heterogeneity in cancer and the search for new cancer genes

David I Heiman, A. McKenna, T. Fennell, 2013, Nature.

Mutational heterogeneity in cancer and the search for new cancer genes

Trevor J Pugh, David I Heiman, A. McKenna, 2014 .

The generation and regional localization of 303 new chromosome 5 sequence-tagged sites.

J. McPherson, E. Nickerson, L. Deaven, 1996, Genomics.

Melanoma genome sequencing reveals frequent PREX2 mutations

Trevor J Pugh, T. Fennell, A. Sivachenko, 2012, Nature.

Mutational heterogeneity in cancer and the search for new cancer genes

Trevor J Pugh, David I Heiman, T. Fennell, 2014 .