Concepedia

Author

Quinten Waisfisz

Amsterdam UMC Location Vrije Universiteit AmsterdamORCID

Also Known As

A Jager, Astrid Irwanto, C. C. van der Pol, C. M. Kets, Clare Turnbull, David Van Den Berg, Jan Cobben, Jason Vollenweider, Jenkins, Mark, Kamila Czene

221

Publications

17.8K

Citations

57

H-Index

137

Concepts

All Affiliations

Amsterdam UMC Location Vrije Universiteit AmsterdamVrije Universiteit AmsterdamAmsterdam University Medical CentersAmsterdam NeuroscienceLeiden University Medical Center
QW

About

Quinten Waisfisz is an author at Amsterdam UMC Location Vrije Universiteit Amsterdam specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

34

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Natural Sciences

6

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Engineering

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1.7K

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Public Health

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Health Sciences

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Quinten Waisfisz

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102

Publications

11.6K

Citations

51

H-Index

YearCitations

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Bjarni J. Vilhjálmsson, Jian Yang, Hilary K. Finucane,

The American Journal of Human Genetics

2015

1.5K

Biallelic Inactivation of <i>BRCA2</i> in Fanconi Anemia

Niall G. Howlett, Toshiyasu Taniguchi, Susan B. Olson,

Science

2002

1.1K

MicroRNA Related Polymorphisms and Breast Cancer Risk

Sofia Khan, Dario Greco, Kyriaki Michailidou,

PLoS ONE

2014

637

A novel ubiquitin ligase is deficient in Fanconi anemia

Amom Ruhikanta Meetei, Johan P. de Winter, Annette L. Medhurst,

Nature Genetics

2003

568

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Marieke Levitus, Quinten Waisfisz, Barbara C. Godthelp,

Nature Genetics

2005

430

Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion

Hugo Vega, Quinten Waisfisz, Miriam Gordillo,

Nature Genetics

2005

384

High Stem Cell Frequency in Acute Myeloid Leukemia at Diagnosis Predicts High Minimal Residual Disease and Poor Survival

Anna van Rhenen, N Feller, Angèle Kelder,

Clinical Cancer Research

2005

370

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Stefan Gräf, Matthias Haimel, Marta Bleda,

Nature Communications

2018

364

The Fanconi anaemia group G gene FANCG is identical with XRCC9

Johan P. de Winter, Quinten Waisfisz, Martin A. Rooimans,

Nature Genetics

1998

355

The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

Johan P. de Winter, Martin A. Rooimans, Laura van der Weel,

Nature Genetics

2000

271

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