Hermine E. Veenstra‐Knol

2.7k total citations
20 papers, 561 citations indexed

About

Hermine E. Veenstra‐Knol is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Hermine E. Veenstra‐Knol has authored 20 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Hermine E. Veenstra‐Knol's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (3 papers). Hermine E. Veenstra‐Knol is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (3 papers). Hermine E. Veenstra‐Knol collaborates with scholars based in Netherlands, United States and Germany. Hermine E. Veenstra‐Knol's co-authors include Anthonie J. van Essen, J. Peter van Tintelen, Arthur van den Wijngaard, Robert M.W. Hofstra, Conny M.A. van Ravenswaaij‐Arts, Birgit Sikkema‐Raddatz, Johanna C. Herkert, Richard J. Sinke, Jan D.H. Jongbloed and Albert J.H. Suurmeijer and has published in prestigious journals such as The American Journal of Human Genetics, Cardiovascular Research and European Journal of Cancer.

In The Last Decade

Hermine E. Veenstra‐Knol

19 papers receiving 553 citations

Peers

Countries citing papers authored by Hermine E. Veenstra‐Knol

Since Specialization

Citations

This map shows the geographic impact of Hermine E. Veenstra‐Knol's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hermine E. Veenstra‐Knol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hermine E. Veenstra‐Knol more than expected).

Fields of papers citing papers by Hermine E. Veenstra‐Knol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hermine E. Veenstra‐Knol. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hermine E. Veenstra‐Knol. The network helps show where Hermine E. Veenstra‐Knol may publish in the future.

Co-authorship network of co-authors of Hermine E. Veenstra‐Knol

This figure shows the co-authorship network connecting the top 25 collaborators of Hermine E. Veenstra‐Knol. A scholar is included among the top collaborators of Hermine E. Veenstra‐Knol based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hermine E. Veenstra‐Knol. Hermine E. Veenstra‐Knol is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Expanding the phenotype of anauxetic dysplasia caused by biallelic NEPRO mutations: A case report 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Jan D.H. Jongbloed, Peter C. van den Akker, Hermine E. Veenstra‐Knol, Marrit M. Hitzert	2
2	Diagnostic Gene Panel Testing in (Non)-Syndromic Patients with Cleft Lip, Alveolus and/or Palate in the Netherlands 2023 ·Molecular Syndromology ·(unknown), (unknown), M. F. van Dooren, Augusta M.A. Lachmeijer, Virginie J. M. Verhoeven, Johanna M. van Hagen, (unknown), (unknown), Saskia Koene, Saskia M. Maas, Hermine E. Veenstra‐Knol, Hans Kristian Ploos van Amstel, Maarten P.G. Massink, Aebele B. Mink van der Molen, (unknown)	3
3	A novel mutation in PTHLH in a family with a variable phenotype with brachydactyly, short stature, oligodontia and developmental delay 2023 ·Bone Reports ·(unknown), Hermine E. Veenstra‐Knol, Annemieke M. Boot	3
4	De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability 2020 ·European Journal of Human Genetics ·(unknown), Hermine E. Veenstra‐Knol, Fleur Vansenne, Erica H. Gerkes, (unknown), Yvonne J. Vos, Marina A.J. Tijssen, Deborah A. Sival, Niklas Darín, Els K. Vanhoutte, Mayke Oosterloo, Maartje Pennings, Bart P.C. van de Warrenburg, Erik-Jan Kamsteeg	8
5	EHMT1 mosaicism in apparently unaffected parents is associated with autism spectrum disorder and neurocognitive dysfunction 2018 ·Molecular Autism ·(unknown), (unknown), J.I.M. Egger, Joost Janzing, Nicole de Leeuw, Hermine E. Veenstra‐Knol, Nicolette S. den Hollander, Hans van Bokhoven, Wouter Staal, Tjitske Kleefstra	17
6	Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3 2018 ·The American Journal of Human Genetics ·Sophia Cameron‐Christie, Constance Wells, Marleen Simon, Marja W. Wessels, (unknown), Wenhua Wei, (unknown), (unknown), Sarah A. Sandaradura, David Sillence, Marie‐Pierre Cordier, Hermine E. Veenstra‐Knol, Matteo Cassina, Kathrin Ludwig, Eva Trevisson, Melanie Bahlo, David Markie, Zandra A. Jenkins, Stephen P. Robertson	22
7	Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly 2015 ·BMC Medical Genomics ·Patrick Rump, (unknown), Krista K. van Dijk-Bos, Lennart Johansson, Anthonie J. van Essen, (unknown), Hermine E. Veenstra‐Knol, E. Redeker, Marcel M. A. M. Mannens, Morris A. Swertz, Behrooz Z. Alizadeh, Conny M.A. van Ravenswaaij‐Arts, Richard J. Sinke, Birgit Sikkema‐Raddatz	59
8	Central 22q11.2 deletions 2014 ·American Journal of Medical Genetics Part A ·Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren‐Bemelmans, Hermine E. Veenstra‐Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, William Reardon, Sonja de Munnik, (unknown), Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema‐Raddatz, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts	43
9	Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease 2013 ·European Journal of Human Genetics ·Marie José Stasia, (unknown), Cécile Martel, Véronique Satre, Charles Coutton, Florence Amblard, Gaëlle Vieville, Joris M. van Montfrans, Jaap Jan Boelens, Hermine E. Veenstra‐Knol, Karen M. van Leeuwen, Martin de Boer, Jean‐Paul Brion, Dirk Roos	14
10	Dysmorphic features in 2-year-old IVF/ICSI offspring 2012 ·Early Human Development ·Jorien Seggers, M.L. Haadsma, Arend F. Bos, Maas Jan Heineman, Paul Keating, Jack J. Middelburg, (unknown), Hermine E. Veenstra‐Knol, Joke H. Kok, Jan Maarten Cobben, Mijna Hadders‐Algra	9
11	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010) 2011 ·Cardiovascular Research ·Cornelis J. Boogerd, Dennis Dooijes, Aho Ilgun, Inge B. Mathijssen, Roel Hordijk, Ingrid M.B.H. van de Laar, Patrick Rump, Hermine E. Veenstra‐Knol, Antoon F.M. Moorman, Phil Barnett, Alex V. Postma	0
12	Practical guidelines for interpreting copy number gains detected by high-resolution array in routine diagnostics 2011 ·European Journal of Human Genetics ·(unknown), Birgit Sikkema‐Raddatz, Gerben van der Vries, Trijnie Dijkhuizen, Roel Hordijk, Anthonie J. van Essen, Hermine E. Veenstra‐Knol, Wilhelmina S. Kerstjens‐Frederikse, Johanna C. Herkert, Erica H. Gerkes, (unknown), Klaas Kok, Richard J. Sinke, Conny M.A. van Ravenswaaij‐Arts	52
13	A rare cause of congenital adrenal hyperplasia: Antley-Bixler syndrome due to POR deficiency. 2011 ·PubMed ·Johanna C. Herkert, (unknown), A. Hoek, Hermine E. Veenstra‐Knol, Ido P. Kema, Wiebke Arlt, (unknown)	9
14	Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: Case series, review and follow-up guidelines 2011 ·European Journal of Cancer ·Johanna C. Herkert, Renée C. Niessen, (unknown), Hermine E. Veenstra‐Knol, Yvonne J. Vos, Heleen M. van der Klift, René Scheenstra, Carli M.J. Tops, Arend Karrenbeld, Frans Peters, Robert M.W. Hofstra, Jan H. Kleibeuker, Rolf H. Sijmons	49
15	Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome 2010 ·Cardiovascular Research ·Cornelis J. Boogerd, Dennis Dooijes, Aho Ilgun, Inge B. Mathijssen, Roel Hordijk, Ingrid M.B.H. van de Laar, (unknown), Hermine E. Veenstra‐Knol, Antoon F.M. Moorman, Phil Barnett, Alex V. Postma	34
16	Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene 2009 ·Heart Rhythm ·J. Peter van Tintelen, Isabelle C Van Gelder, Angeliki Asimaki, Albert J.H. Suurmeijer, Ans C.P. Wiesfeld, Jan D.H. Jongbloed, Arthur van den Wijngaard, Jan B. M. Kuks, Karin Y. van Spaendonck‐Zwarts, Nicolette C. Notermans, Ludolf G. Boven, Freek van den Heuvel, Hermine E. Veenstra‐Knol, Jeffrey E. Saffitz, Robert M.W. Hofstra, Maarten P. van den Berg	117
17	Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene 2007 ·European Journal of Medical Genetics ·Jorieke E. H. Bergman, Hermine E. Veenstra‐Knol, Anthonie J. van Essen, Conny M.A. van Ravenswaaij, Wilfred F.A. den Dunnen, Arthur van den Wijngaard, J. Peter van Tintelen	30
18	Early recognition of basal cell naevus syndrome 2004 ·European Journal of Pediatrics ·Hermine E. Veenstra‐Knol, (unknown), (unknown), (unknown), Margreet G.E.M. Ausems	33
19	Genotype-Phenotype Correlation in Patients Suspected of Having Sotos Syndrome 2004 ·Hormone Research in Paediatrics ·Lonneke de Boer, Sarina G. Kant, Marcel Karperien, (unknown), Jennifer M.L. Tjon, Geraldine R. Vink, (unknown), Hans G. Dauwerse, Saskia le Cessie, Frits A. Beemer, Ineke van der Burgt, Ben C.J. Hamel, Raoul C. M. Hennekam, Ursula Kuhnle, Inge B. Mathijssen, Hermine E. Veenstra‐Knol, (unknown), Martijn H. Breuning, Jan M. Wit	43
20	Unreported manifestations in two Dutch families with Bartsocas–Papas syndrome 2003 ·American Journal of Medical Genetics Part A ·Hermine E. Veenstra‐Knol, (unknown), Albertus Timmer, Leo P. ten Kate, Anthonie J. van Essen	14

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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