Hanka Venselaar

9.2k citations

87 papers · 3.4k indexed · 1 hit paper · h-index 32

Co-authors: Gert Vriend Maarten L. Hekkelman Remko Kuipers Martijn A. Huynen Jan Smeıtınk Joost G.J. Hoenderop René J.M. Bindels Leo Nijtmans
Topics: Hearing, Cochlea, Tinnitus, Genetics (9 papers)Genomics and Rare Diseases (8 papers)Mitochondrial Function and Pathology (7 papers)
Cited by: Sensory Systems Clinical Biochemistry Molecular Biology
Journals: Proceedings of the National Academy of Sciences Journal of the American Chemical Society Nucleic Acids Research
Partner nations: Netherlands Germany United States

In The Last Decade

Hanka Venselaar

86 papers receiving 3.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces

2010 765 citations Hanka Venselaar, Gert Vriend et al. profile →

Peers

Countries citing papers authored by Hanka Venselaar

Since Specialization

Citations

This map shows the geographic impact of Hanka Venselaar'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 Hanka Venselaar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hanka Venselaar more than expected).

Fields of papers citing papers by Hanka Venselaar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hanka Venselaar. 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 Hanka Venselaar. The network helps show where Hanka Venselaar may publish in the future.

Co-authorship network of co-authors of Hanka Venselaar

This figure shows the co-authorship network connecting the top 25 collaborators of Hanka Venselaar. A scholar is included among the top collaborators of Hanka Venselaar 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 Hanka Venselaar. Hanka Venselaar 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	A rare homozygous INS variant causes adult-onset diabetes 2024 ·BMJ Open Diabetes Research & Care ·(unknown),Tine Glendorf,Antonius E. van Herwaarden,Hanka Venselaar,(unknown),Ron A. Wevers,Jolein Gloerich,Alain J. van Gool,Cees J. Tack	0
2	A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for USH2A-associated retinitis pigmentosa 2023 ·Molecular Therapy — Nucleic Acids ·(unknown),Sanne Broekman,Theo Peters,(unknown),(unknown),Hanka Venselaar,Hannie Kremer,Erik de Vrieze,Erwin van Wijk	8
3	Novel α-1,3-Glucosyltransferase Variants and Their Broad Clinical Polycystic Liver Disease Spectrum 2023 ·Genes ·(unknown),René H. M. te Morsche,Hanka Venselaar,(unknown),Anja Geerts,Anne Hoorens,Joost P.H. Drenth	1
4	Aggregation of population‐based genetic variation over protein domain homologues and its potential use in genetic diagnostics 2017 ·Human Mutation ·Laurens Wiel,Hanka Venselaar,Joris A. Veltman,Gert Vriend,Christian Gilissen	20
5	Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes 2017 ·The American Journal of Human Genetics ·Stefan H. Lelieveld,Laurens Wiel,Hanka Venselaar,Rolph Pfundt,Gerrit Vriend,Joris A. Veltman,Han G. Brunner,Lisenka E.L.M. Vissers,Christian Gilissen	46
6	Therapeutic NOTCH3 cysteine correction in CADASIL using exon skipping:in vitroproof of concept 2016 ·Brain ·Julie W. Rutten,Hans G. Dauwerse,Dorien J.M. Peters,(unknown),Hanka Venselaar,Christof Haffner,Gert‐Jan B. van Ommen,Annemieke Aartsma‐Rus,Saskia A.J. Lesnik Oberstein	41
7	Nonsyndromic Hearing Loss Caused by USH1G Mutations 2014 ·Ear and Hearing ·(unknown),Ramon A. C. van Huet,(unknown),Jaap Oostrik,Hanka Venselaar,Erwin van Wijk,Andy J. Beynon,Henricus P. M. Kunst,Carel B. Hoyng,Hannie Kremer,Margit Schraders,Ronald J. E. Pennings	20
8	A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine 2014 ·European Journal of Human Genetics ·Se‐Kyung Oh,Jeong‐In Baek,(unknown),Hanka Venselaar,Herman G.P. Swarts,Seong‐Hyun Park,Muhammad Hashim Raza,Da Jung Jung,Soo‐Young Choi,Sang‐Heon Lee,Thomas Friedrich,Gert Vriend,Jan J. Koenderink,Un‐Kyung Kim,Kyu-Yup Lee	19
9	Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions 2013 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Herman G.P. Swarts,(unknown),Hanka Venselaar,Arn M. J. M. van den Maagdenberg,Frans G. M. Rüssel,Jan J. Koenderink	15
10	Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone Dysfunction 2013 ·Ophthalmology ·Susanne Roosing,L. Ingeborgh van den Born,Carel B. Hoyng,Alberta A. H. J. Thiadens,Elfride De Baere,Rob W.J. Collin,(unknown),Bart Leroy,(unknown),Hanka Venselaar,Frans C. C. Riemslag,Frans P.M. Cremers,Caroline C. W. Klaver,Anneke I. den Hollander	29
11	Bacterial CS2 Hydrolases from Acidithiobacillus thiooxidans Strains Are Homologous to the Archaeal Catenane CS2 Hydrolase 2013 ·Journal of Bacteriology ·Marjan J. Smeulders,Arjan Pol,Hanka Venselaar,Thomas R. M. Barends,(unknown),Mike S. M. Jetten,Huub J. M. Op den Camp	27
12	Mutations in PCBD1 Cause Hypomagnesemia and Renal Magnesium Wasting 2013 ·Journal of the American Society of Nephrology ·Silvia Ferrè,Jeroen H. F. de Baaij,Patrick Ferreira,(unknown),Johannis B.C. de Klerk,Marla Lavrijsen,Femke van Zeeland,Hanka Venselaar,Leo A. J. Kluijtmans,Joost G.J. Hoenderop,René J.M. Bindels	54
13	A catalytic defect in mitochondrial respiratory chain complex I due to a mutation in NDUFS2 in a patient with Leigh syndrome 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Lock Hock Ngu,Leo Nijtmans,Felix Distelmaier,Hanka Venselaar,Sjenet E. van Emst‐de Vries,Mariël A.M. van den Brand,(unknown),Liesbeth T. Wintjes,Peter H.G.M. Willems,Lambertus P. van den Heuvel,Jan Smeıtınk,Richard J. Rodenburg	27
14	Chondrodysplasia and Abnormal Joint Development Associated with Mutations in IMPAD1, Encoding the Golgi-Resident Nucleotide Phosphatase, gPAPP 2011 ·The American Journal of Human Genetics ·Lisenka E.L.M. Vissers,Ekkehart Lausch,Sheila Unger,Belinda Campos‐Xavier,Christian Gilissen,Antonio Rossi,Marisol del Rosario,Hanka Venselaar,Ute Knoll,Sheela Nampoothiri,Mohandas Nair,Jürgen W. Spranger,Han G. Brunner,Luisa Bonafé,Joris A. Veltman,Bernhard Zabel,Andrea Superti‐Furga	66
15	The structure–function relationship of the Aspergillus fumigatus cyp51A L98H conversion by site-directed mutagenesis: The mechanism of L98H azole resistance 2011 ·Fungal Genetics and Biology ·Eveline Snelders,Anna Karawajczyk,(unknown),Hanka Venselaar,Gijs Schaftenaar,Paul E. Verweij,Willem J. G. Melchers	91
16	Mass Spectrometry Analysis of Hepcidin Peptides in Experimental Mouse Models 2011 ·PLoS ONE ·Harold Tjalsma,Coby M. Laarakkers,Rachel P. L. van Swelm,Milan Theurl,Igor Theurl,Erwin Kemna,Yuri E. M. van der Burgt,Hanka Venselaar,Bas E. Dutilh,Frans G. M. Rüssel,Günter Weiß,Rosalinde Masereeuw,Robert E. Fleming,Dorine W. Swinkels	24
17	Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP 2010 ·Human Mutation ·Konstantinos Nikopoulos,Hanka Venselaar,Rob W.J. Collin,Rosa Riveiro-Álvarez,F. Nienke Boonstra,Johanna M. M. Hooymans,Arijit Mukhopadhyay,Deborah Shears,(unknown),Ilse J. de Wijs,Anthonie J. van Essen,Rolf H. Sijmons,M. A. D. Tilanus,(unknown),Carmen Ayuso,(unknown),Frans P.M. Cremers	121
18	Role of the α-Kinase Domain in Transient Receptor Potential Melastatin 6 Channel and Regulation by Intracellular ATP 2008 ·Journal of Biological Chemistry ·Stéphanie Thebault,Gang Cao,Hanka Venselaar,Qi Xi,René J.M. Bindels,Joost G.J. Hoenderop	44
19	A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients 2007 ·Blood Cells Molecules and Diseases ·Dorine W. Swinkels,Hanka Venselaar,Erwin T. Wiegerinck,Egbert Bakker,Irma Joosten,(unknown),(unknown),Martijn H. Breuning	9
20	Negative Constraints Underlie the ErbB Specificity of Epidermal Growth Factor-like Ligands 2006 ·Journal of Biological Chemistry ·(unknown),(unknown),Sander B. Nabuurs,Hanka Venselaar,(unknown),(unknown),Gert Vriend,Catelijne Stortelers,E.J.J. van Zoelen	5

About Hanka Venselaar

Hanka Venselaar is a scholar working on Sensory Systems, Genetics and Molecular Biology, having authored 87 papers that have together received 3.4k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Genomics and Rare Diseases (8 papers) and Mitochondrial Function and Pathology (7 papers). The work is most often cited by research in Sensory Systems (265 citations), Clinical Biochemistry (285 citations) and Molecular Biology (2.1k citations). Hanka Venselaar has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Gert Vriend, Maarten L. Hekkelman, Remko Kuipers, Martijn A. Huynen, Jan Smeıtınk, Joost G.J. Hoenderop, René J.M. Bindels, Leo Nijtmans, Richard J. Rodenburg and Christian Gilissen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

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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