Gertjan van Ommen

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2020
Позовавания	66951	11904
h-индекс	117	52
i10-индекс	398	156

3500

1750

875

2625

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Публичен достъп

Преглед на всички

43 статии

6 статии

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

Peter A.C. 't HoenProfessor Bioinformatics, Centre for Molecular and Biomolecular Informatics, Radboudumc NijmegenПотвърден имейл адрес: radboudumc.nl
Peter PearsonVisiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao PauloПотвърден имейл адрес: ib.usp.br
Marten HofkerProfessor of Molecular Genetics, UMCG, Groningen University, The NetherlandsПотвърден имейл адрес: umcg.nl
Silvère van der MaarelProfessor of Medical Epigenetics, Head of Department, Human Genetics, Leiden University MedicalПотвърден имейл адрес: lumc.nl
Martin C WapenaarПотвърден имейл адрес: umcg.nl
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theПотвърден имейл адрес: umcg.nl
P. Eline SlagboomProfessor Molecular Epidemiology, Leiden University Medical CenterПотвърден имейл адрес: lumc.nl
Antoon MoormanDepartment of Medical Biology, AMC, AmsterdamПотвърден имейл адрес: amsterdamumc.nl
Rachel H. GilesUniversity Medical Center UtrechtПотвърден имейл адрес: umcutrecht.nl
Jan C. OosterwijkClinical Geneticist, MD, PhDПотвърден имейл адрес: umcg.nl
Marian BeekmanAssistant Professor, Molecular Epidemiology, LUMCПотвърден имейл адрес: lumc.nl
J van kriekenhoogleraar pathologie, UMC St RadboudПотвърден имейл адрес: radboudumc.nl
Marjolein KriekLUMCПотвърден имейл адрес: lumc.nl
Stefan WhiteWhiteFox Science ConsultingПотвърден имейл адрес: whitefoxsc.com
Paul I W de BakkerVertex PharmaceuticalsПотвърден имейл адрес: vrtx.com
Markus Perolaresearch professorПотвърден имейл адрес: thl.fi
Morris SwertzFull Professor / Head of Genomics Coordination Center, Dept of Genetics, University MedicalПотвърден имейл адрес: rug.nl
Vishna Devi NadarajahNewcastle University Medicine Malaysia, Newcastle UniversityПотвърден имейл адрес: newcastle.edu.my
Anthony P MonacoPresident, Tufts UniversityПотвърден имейл адрес: tufts.edu
Niels TommerupProfessor in Medical Genetics, University of CopenhagenПотвърден имейл адрес: sund.ku.dk

Следене

Gertjan van Ommen

Professor in Human Genetics, Leiden University Medical Centre

Потвърден имейл адрес: lumc.nl

Genetics Genomics Duchenne Gene therapy Biobanking


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
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	4330	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), 937-948, 2010	3646	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	2954	1996
Hundreds of variants clustered in genomic loci and biological pathways affect human height H Lango Allen, K Estrada, G Lettre, SI Berndt, MN Weedon, F Rivadeneira, ... Nature 467 (7317), 832-838, 2010	2352	2010
Transcriptome and genome sequencing uncovers functional variation in humans T Lappalainen, M Sammeth, MR Friedländer, PAC ‘t Hoen, J Monlong, ... Nature 501 (7468), 506-511, 2013	2132	2013
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), 348-351, 1995	1514	1995
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	1285	1989
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), 949-960, 2010	1137	2010
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	1073	2007
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	925	2011
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	845	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	800	2010
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	788	2008
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), 26-30, 1992	774	1992
Theoretic applicability of antisense‐mediated exon skipping for Duchenne muscular dystrophy mutations A Aartsma‐Rus, I Fokkema, J Verschuuren, I Ginjaar, J Van Deutekom, ... Human mutation 30 (3), 293-299, 2009	748	2009
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	743	2008
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014	739	2014
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	698	1989
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit JCTV Deutekom, C Wljmenga, EAEV Tlenhoven, AM Gruter, JE Hewitt, ... Human molecular genetics 2 (12), 2037-2042, 1993	610	1993
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy LM Kunkel, co-authors Nature 322 (6074), 73-77, 1986	582	1986

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