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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Alan Pittman

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2021

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotypeSatyamaanasa Polubothu, Davide Zecchin, Lara Al-Olabi, et al.

Genome Research|September 10, 2017

Detection of long repeat expansions from PCR-free whole-genome sequence dataEgor Dolzhenko, Joke J F A van Vugt, Richard J Shaw, et al.

Nature Genetics|December 20, 2016

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.

Nature Communications|September 1, 2022

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathwaysWilliam J Young, Najim Lahrouchi, Aaron Isaacs, et al.

Nature Genetics|July 26, 2016

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.

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Search research articles

Showing results (51-60 of 55) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 55 results.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2021

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotypeSatyamaanasa Polubothu, Davide Zecchin, Lara Al-Olabi, et al.

Genome Research|September 10, 2017

Detection of long repeat expansions from PCR-free whole-genome sequence dataEgor Dolzhenko, Joke J F A van Vugt, Richard J Shaw, et al.

Nature Genetics|December 20, 2016

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.

Nature Communications|September 1, 2022

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathwaysWilliam J Young, Najim Lahrouchi, Aaron Isaacs, et al.

Nature Genetics|July 26, 2016

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.

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