Ans M. W. van den Ouweland

Overview

Best Publications

• Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34

  Marjon van Slegtenhorst;Ronald de Hoogt;Caroline Hermans;Mark Nellist

  1817
  Citations

• Association analysis identifies 65 new breast cancer risk loci

  Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley

  1400
  Citations

• Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation

  Hanne Meijers-Heijboer;Bert van Geel;Wim L.J. van Putten;Sonja C. Henzen-Logmans

  1350
  Citations

• Genome-wide association study identifies five new breast cancer susceptibility loci

  Clare Turnbull;Shahana Ahmed;Jonathan Morrison;David Pernet

  843
  Citations

• Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders.

  Bethan Jones;Emma L. Jones;Stephanie A. Bonney;Hetal N. Patel

  438
  Citations

• A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases

  Kornelia Neveling;Ilse Feenstra;Christian Gilissen;Lies H. Hoefsloot

  430
  Citations

• Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

  Roger L Milne;Roger L Milne;Karoline B Kuchenbaecker;Karoline B Kuchenbaecker;Kyriaki Michailidou;Kyriaki Michailidou;Jonathan Beesley

  376
  Citations

• Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

  Haoyu Zhang;Haoyu Zhang;Thomas U. Ahearn;Julie Lecarpentier;Daniel Barnes

  374
  Citations

• MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

  Nelly Burnichon;Alberto Cascón;Francesca Schiavi;Nicole Paes Morales

  361
  Citations

• Genome-wide association analysis identifies three new breast cancer susceptibility loci

  Maya Ghoussaini;Olivia Fletcher;Kyriaki Michailidou;Clare Turnbull

  359
  Citations

• Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

  Arjen R. Mensenkamp;Ingrid P. Vogelaar;Wendy A.G. van Zelst–Stams;Monique Goossens

  352
  Citations

• Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis

  D.L. Smit;Arjen Mensenkamp;S. Badeloe;Martijn Breuning

  223
  Citations

• Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk

  Sanne W. ten Broeke;Richard M. Brohet;Carli M. Tops;Heleen M. van der Klift

  218
  Citations

• PACSINs Bind to the TRPV4 Cation Channel PACSIN 3 MODULATES THE SUBCELLULAR LOCALIZATION OF TRPV4

  Math P. Cuajungco;Christian Grimm;Kazuo Oshima;Dieter D'hoedt

  196
  Citations

• Cancer Risks for PMS2-Associated Lynch Syndrome

  Sanne W Ten Broeke;Heleen M van der Klift;Carli M J Tops;Stefan Aretz

  188
  Citations

• Direct interaction with Rab11a targets the epithelial Ca2+ channels TRPV5 and TRPV6 to the plasma membrane.

  Stan F. J. van de Graaf;Qing Chang;Arjen R. Mensenkamp;Joost G. J. Hoenderop

  181
  Citations

• Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders

  Rolph Pfundt;Marisol del Rosario;Lisenka E.L.M. Vissers;Michael P. Kwint

  175
  Citations

• Apolipoprotein E Participates in the Regulation of Very Low Density Lipoprotein-Triglyceride Secretion by the Liver

  A R Mensenkamp;M C Jong;van Harry Goor;van Marja Luyn

  162
  Citations

• Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

  Mia M. Gaudet;Karoline B. Kuchenbaecker;Joseph Vijai;Robert J. Klein

  159
  Citations

• Calbindin-D28K dynamically controls TRPV5-mediated Ca2+ transport.

  Tim T Lambers;Frank Mahieu;Elena Oancea;Louis Hoofd

  156
  Citations