Eric A. M. Hennekam

1.9k citations

14 papers · 957 indexed · h-index 11

Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 4
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
Neurology top 10%
- Amyotrophic Lateral Sclerosis Research 4
Oral Surgery top 5%
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
Cognitive Neuroscience
- Autism Spectrum Disorder Research 2
Cell Biology
- Skin and Cellular Biology Research 1
Molecular Biology
- Prion Diseases and Protein Misfolding 1
Oncology
- Drug Transport and Resistance Mechanisms 1

Co-authors: Jan H. Veldink Leonard H. van den Berg Helenius J. Schelhaas Michael A. van Es Dick Lindhout Pierre R. Bourque Marka van Blitterswijk Anneke J. van der Kooi
Cited by: Neurology Genetics
Journals: Nature Genetics (1 paper)PLoS ONE (1 paper)Neurology (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

Eric A. M. Hennekam

13 papers receiving 943 citations

Peers

Countries citing papers authored by Eric A. M. Hennekam

Since Specialization

Citations

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

Fields of papers citing papers by Eric A. M. Hennekam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric A. M. Hennekam. 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 Eric A. M. Hennekam. The network helps show where Eric A. M. Hennekam may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Eric A. M. Hennekam, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eric A. M. Hennekam Line = papers co-authored together Eric A. M. Hennekam links everyone, so they are left out of the graph.

All Works

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14 of 14 papers shown

#	Work
1	Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene Journal of Human Genetics ·Irma van de Beek,Iris Glykofridis,Michael W.T. Tanck,Monique Luijten,Theo M. Starink,Jesper A. Balk,Paul C. Johannesma,Eric A. M. Hennekam,Maurice J.B. van den Hoff,Quinn D. Gunst,Gilles Thomas,Abeltje M. Polstra,Pieter E. Postmus,Maurice A. M. Van Steensel,Alex V. Postma,Rob M.F. Wolthuis,Fred H. Menko,Arjan C. Houweling,Quinten Waisfisz	2023	5
2	Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia Nephrology Dialysis Transplantation ·Jeroen H. F. de Baaij,Eiske M. Dorresteijn,Eric A. M. Hennekam,E.-J. Kamsteeg,R. Meijer,Karin Dahan,Michelle Müller,Marinus A. van den Dorpel,René J.M. Bindels,Joost G.J. Hoenderop,Olivier Devuyst,Nine Knoers	2015	41
3	Increased paternal age and the influence on burden of genomic copy number variation in the general population Human Genetics ·Jacobine E. Buizer‐Voskamp,Hylke M. Blauw,Marco P. Boks,Kristel R. van Eijk,Jan H. Veldink,Eric A. M. Hennekam,Jacob Vorstman,Flip Mulder,Henning Tiemeier,André G. Uitterlinden,Lambertus A. Kiemeney,Leonard H. van den Berg,René S. Kahn,Chiara Sabatti,Roel A. Ophoff	2013	29
4	Genetic Overlap between Apparently Sporadic Motor Neuron Diseases PLoS ONE ·Marka van Blitterswijk,Lotte Vlam,Michael A. van Es,W. Ludo van der Pol,Eric A. M. Hennekam,Dennis Dooijes,Helenius J. Schelhaas,Anneke J. van der Kooi,Marianne de Visser,Jan H. Veldink,Leonard H. van den Berg	2012	51
5	Evidence for an oligogenic basis of amyotrophic lateral sclerosis Human Molecular Genetics ·Marka van Blitterswijk,Michael A. van Es,Eric A. M. Hennekam,Dennis Dooijes,Wouter van Rheenen,Jelena Medic,Pierre R. Bourque,Helenius J. Schelhaas,Anneke J. van der Kooi,Marianne de Visser,Paul I.W. de Bakker,Jan H. Veldink,Leonard H. van den Berg	2012	237
6	Familial clustering of schizophrenia, bipolar disorder, and major depressive disorder Genetics in Medicine ·Maartje F. Aukes,Wijnand Laan,Fabian Termorshuizen,Jacobine E. Buizer‐Voskamp,Eric A. M. Hennekam,Hugo M. Smeets,Roel A. Ophoff,Marco P. Boks,René S. Kahn	2012	17
7	Mutations in WNT10A are present in more than half of isolated hypodontia cases Journal of Medical Genetics ·Marie-José van den Boogaard,Marijn Créton,Yvon Bronkhorst,Annemieke van der Hout,Eric A. M. Hennekam,Dick Lindhout,Marco S. Cune,Hans Kristian Ploos van Amstel	2012	163
8	Parental age and the risk of amyotrophic lateral sclerosis Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Sonja W. de Jong,Mark Huisman,Eric A. M. Hennekam,Nadia A. Sutedja,Anneke J. van der Kooi,Marianne de Visser,H. Jurgen Schelhaas,Kathelijn Fischer,Jan H. Veldink,Leonard H. van den Berg	2012	0
9	A novel Dutch mutation in UNC13D reveals an essential role of the C2B domain in munc13‐4 function Pediatric Blood & Cancer ·Edo Elstak,D. Maroeska W. M. te Loo,Kiki Tesselaar,Peter van Kerkhof,Jan Loeffen,Dimitrios Grivas,Eric A. M. Hennekam,Jaap Jan Boelens,Peter M. Hoogerbrugge,Peter van der Sluijs,Mariëlle van Gijn,Lisette van de Corput	2011	8
10	Paternal age and psychiatric disorders: Findings from a Dutch population registry Schizophrenia Research ·Jacobine E. Buizer‐Voskamp,Wijnand Laan,Wouter Staal,Eric A. M. Hennekam,Maartje F. Aukes,Fabian Termorshuizen,René S. Kahn,Marco P. Boks,Roel A. Ophoff	2011	67
11	A double hit implicates DIAPH3 as an autism risk gene Molecular Psychiatry ·J.A.S. Vorstman,Emma van Daalen,G R Jalali,Ewoud R.E. Schmidt,R. Jeroen Pasterkamp,M de Jonge,Eric A. M. Hennekam,Eva Tiensuu Janson,Wouter Staal,B. van der Zwaag,J. Peter H. Burbach,R.S. Kahn,Beverly S. Emanuel,Hermán van Engeland,RA Ophoff	2010	51
12	Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans Nature Genetics ·Mariëlle Alders,Benjamin M. Hogan,Evisa Gjini,Faranak Salehi,Lihadh Al‐Gazali,Eric A. M. Hennekam,Eva Holmberg,Marcel M. A. M. Mannens,Margot F. Mulder,G. Johan A. Offerhaus,Trine Prescott,Eelco J. Schroor,Joanne Verheij,Merlijn Witte,Petra Zwijnenburg,Miikka Vikkula,Stefan Schulte‐Merker,Raoul C. M. Hennekam	2009	206
13	A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION Neurology ·Michael A. van Es,Frank P. Diekstra,Jan H. Veldink,Frank Baas,Pierre R. Bourque,Helenius J. Schelhaas,E Strengman,Eric A. M. Hennekam,Dick Lindhout,Roel A. Ophoff,Leonard H. van den Berg	2009	59
14	Autosomal‐recessive inheritance of benign recurrent intrahepatic cholestasis American Journal of Medical Genetics ·Tom J. de Koning,Lodewijk A. Sandkuijl,Jan E. A. R. De Schryver,Eric A. M. Hennekam,Frits A. Beemer,Roderick H.J. Houwen	1995	23

About Eric A. M. Hennekam

Eric A. M. Hennekam is a scholar working on Genetics, Neurology and Speech and Hearing, having authored 14 papers that have together received 957 indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Autism Spectrum Disorder Research (2 papers), Genomics and Rare Diseases (1 paper), Skin and Cellular Biology Research (1 paper), Prion Diseases and Protein Misfolding (1 paper) and Drug Transport and Resistance Mechanisms (1 paper). The work is most often cited by research in Neurology (332 citations), Genetics (230 citations) and Neurology (128 citations). Eric A. M. Hennekam has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Jan H. Veldink, Leonard H. van den Berg, Helenius J. Schelhaas, Michael A. van Es, Dick Lindhout, Pierre R. Bourque, Marka van Blitterswijk, Anneke J. van der Kooi, Dennis Dooijes and Marianne de Visser. Their work appears in journals such as Nature Genetics, PLoS ONE and Neurology.

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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