Gerald Goh

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Medicine, Genetics, Molecular Genetics +17

Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma

Michael Krauthammer, Yong Kong, Byung Hak Ha et al. · Nature Genetics · 2012 · 1.2K citations

Medicine, Genetics, Oncology +12

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

Ute I. Scholl, Gerald Goh, Gabriel Stölting et al. · Nature Genetics · 2013 · 619 citations

Medicine, Endocrinology, Molecular Genetics +16

Genomic landscape of cutaneous T cell lymphoma

Jaehyuk Choi, Gerald Goh, Trent Walradt et al. · Nature Genetics · 2015 · 418 citations · Full text

Medicine, Molecular Genetics, Oncology +14

Mutational landscape of MCPyV-positive and MCPyV-negative Merkel cell carcinomas with implications for immunotherapy

Gerald Goh, Trent Walradt, Vladimir Markarov et al. · Oncotarget · 2015 · 386 citations · Full text

Medicine, Oncology, Pathology +17