Gertjan van Ommen - Citas de Google Académico

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Coautores

Peter PearsonVisiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao PauloDirección de correo verificada de ib.usp.br
Peter A.C. 't HoenProfessor Bioinformatics, Centre for Molecular and Biomolecular Informatics, Radboudumc NijmegenDirección de correo verificada de radboudumc.nl
Marten HofkerProfessor of Molecular Genetics, UMCG, Groningen University, The NetherlandsDirección de correo verificada de umcg.nl
padberg g.w.hoogleraar neurologieDirección de correo verificada de neuro.umcn.nl
Silvère van der MaarelProfessor of Medical Epigenetics, Head of Department, Human Genetics, Leiden University MedicalDirección de correo verificada de lumc.nl
Martin C WapenaarDirección de correo verificada de umcg.nl
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theDirección de correo verificada de umcg.nl
P. Eline SlagboomProfessor Molecular Epidemiology, Leiden University Medical CenterDirección de correo verificada de lumc.nl
Rachel H. GilesUniversity Medical Ceneter UtrechtDirección de correo verificada de umcutrecht.nl
Antoon MoormanDirección de correo verificada de amc.uva.nl
Jan C. OosterwijkClinical Geneticist, MD, PhDDirección de correo verificada de umcg.nl
Marjolein KriekLUMCDirección de correo verificada de lumc.nl
Marian BeekmanSenior Scientist, Molecular Epidemiology, LUMCDirección de correo verificada de lumc.nl
Stefan WhiteWhiteFox Science ConsultingDirección de correo verificada de whitefoxsc.com
Anthony P MonacoPresident, Tufts UniversityDirección de correo verificada de tufts.edu
Barend MonsProfessor in Biosemantics, Leiden universiteit medical center and DTLDirección de correo verificada de dtls.nl
Markus Perolaresearch professorDirección de correo verificada de thl.fi
Roel A. OphoffProfessor of Psychiatry and Human Genetics, University of California Los AngelesDirección de correo verificada de ucla.edu
Vishna Devi NadarajahInternational Medical University, Leiden University Medical centreDirección de correo verificada de imu.edu.my
Esther van de VosseAssistant Professor, Leiden University Medical Center, Leiden, The NetherlandsDirección de correo verificada de LUMC.nl

Gertjan van Ommen

Professor in Human Genetics, Leiden University Medical Centre

Dirección de correo verificada de lumc.nl

Genetics Genomics Duchenne Gene therapy Biobanking


Título	Citado por	Año
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome AJMH Verkerk, M Pieretti, JS Sutcliffe, YH Fu, DPA Kuhl, A Pizzuti, ... Cell 65 (5), 905-914, 1991	3399	1991
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ... Nature genetics 42 (11), 937, 2010	2620	2010
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 RA Ophoff, GM Terwindt, MN Vergouwe, R Van Eijk, PJ Oefner, ... Cell 87 (3), 543-552, 1996	2509	1996
Hundreds of variants clustered in genomic loci and biological pathways affect human height HL Allen, K Estrada, G Lettre, SI Berndt, MN Weedon, F Rivadeneira, ... Nature 467 (7317), 832, 2010	1742	2010
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP F Petrif, RH Giles, HG Dauwerse, JJ Saris, RCM Hennekam, M Masuno, ... Nature 376 (6538), 348, 1995	1307	1995
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, P AC‘t Hoen, J Monlong, ... Nature 501 (7468), 506, 2013	1236	2013
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion M Koenig, AH Beggs, M Moyer, S Scherpf, K Heindrich, T Bettecken, ... American journal of human genetics 45 (4), 498, 1989	1044	1989
No distribution without individuals’ cognition: A dynamic interactional view G Salomon Distributed cognitions: Psychological and educational considerations, 111-138, 1993	999*	1993
Local dystrophin restoration with antisense oligonucleotide PRO051 JC Van Deutekom, AA Janson, IB Ginjaar, WS Frankhuizen, ... New England Journal of Medicine 357 (26), 2677-2686, 2007	925	2007
Child and adolescent psychiatry M Rutter, E Taylor, L Hersov Journal of the American Academy of Child & Adolescent Psychiatry 34 (7), 1995	864*	1995
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution IM Heid, AU Jackson, JC Randall, TW Winkler, L Qi, V Steinthorsdottir, ... Nature genetics 42 (11), 949, 2010	822	2010
Systemic administration of PRO051 in Duchenne's muscular dystrophy NM Goemans, M Tulinius, JT van den Akker, BE Burm, PF Ekhart, ... New England Journal of Medicine 364 (16), 1513-1522, 2011	762	2011
Deep sequencing-based expression analysis shows major advances in robustness, resolution and inter-lab portability over five microarray platforms PAC 't Hoen, Y Ariyurek, HH Thygesen, E Vreugdenhil, RHAM Vossen, ... Nucleic acids research 36 (21), e141-e141, 2008	675	2008
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. JT Den Dunnen, PM Grootscholten, E Bakker, LA Blonden, HB Ginjaar, ... American journal of human genetics 45 (6), 835, 1989	612	1989
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy C Wijmenga, JE Hewitt, LA Sandkuijl, LN Clark, TJ Wright, HG Dauwerse, ... Nature genetics 2 (1), 26, 1992	609	1992
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles CEG Bruder, A Piotrowski, AACJ Gijsbers, R Andersson, S Erickson, ... The American Journal of Human Genetics 82 (3), 763-771, 2008	596	2008
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy LM Kunkel Nature 322 (6074), 73, 1986	515	1986
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome U Francke, HD Ochs, B de Martinville, J Giacalone, V Lindgren, ... American journal of human genetics 37 (2), 250, 1985	505	1985
Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading‐frame rule A Aartsma‐Rus, JCT Van Deutekom, IF Fokkema, GJB Van Ommen, ... Muscle & Nerve: Official Journal of the American Association of …, 2006	501	2006
A unifying genetic model for facioscapulohumeral muscular dystrophy RJLF Lemmers, PJ Van der Vliet, R Klooster, S Sacconi, P Camaño, ... Science 329 (5999), 1650-1653, 2010	480	2010

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