Klaartje van Engelen

Author

Amsterdam UMC Location University of Amsterdam ORCID

Also Known As

Amanda Ewart Toland, Annemieke H. van der Hout, Carole Brewer, Julian Adlard, K Engelen, K Van Engelen, K. Engelen, K. Van Engelen, K. van Engelen, Klaartje Van Engelen

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam Leiden University Medical Center University Medical Center Utrecht Radboud University Nijmegen University Medical Center Groningen

About

Klaartje van Engelen is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	527
2	Public Health	2	2	51
3	Cardiothoracic Surgery	1	1	28
4	Cell Biology	1	1	43
5	Child Development	1	1	29

Klaartje van Engelen

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Breast cancer risk in transgender people receiving hormone treatment: nationwide cohort study in the Netherlands Christel J.M. de Blok, Chantal M Wiepjes, Nienke M. Nota, BMJ	2019	346
Mutations in the Sarcomere Gene <i>MYH7</i> in Ebstein Anomaly Alex V. Postma, Klaartje van Engelen, Judith van de Meerakker, Circulation Cardiovascular Genetics	2010	186
Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers Bernadette A. M. Heemskerk‐Gerritsen, Agnes Jager, Linetta B. Koppert, Breast Cancer Research and Treatment	2019	181
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Heather J. Cordell, Jamie Bentham, Ana Töpf, Nature Genetics Atrial Septal DefectGenome-wide Association StudyGenetic DisorderGeneticsGenetic Epidemiology	2013	156
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants Daniel R. Barnes, Matti A. Rookus, Lesley McGuffog, Genetics in Medicine	2020	137
Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans Bernard Thienpont, Litu Zhang, Alex V. Postma, The American Journal of Human Genetics Heart FailureDevelopmental BiologyCardiovascular DiseasePhysiologyAdult Congenital Heart Disease	2010	110
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot Heather J. Cordell, Ana Töpf, Chrysovalanto Mamasoula, Human Molecular Genetics	2013	103
Endometrial Cancer Risk in Women With Germline <i>BRCA1</i> or <i>BRCA2</i> Mutations: Multicenter Cohort Study Marthe M. de Jonge, Cor D. de Kroon, Denise J. Jenner, JNCI Journal of the National Cancer Institute	2021	88
Height and Body Mass Index as Modifiers of Breast Cancer Risk in <i>BRCA1</i>/<i>2</i> Mutation Carriers: A Mendelian Randomization Study Frank Qian, Shengfeng Wang, Jonathan S. Mitchell, JNCI Journal of the National Cancer Institute	2018	74
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy Mike Gerards, Bianca van den Bosch, Chantal Calis, Mitochondrion Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2010	72

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