Peter Heutink

59.8k citations

241 papers · 17.9k · 5 hit papers · h-index 62

Impact in

Neurology top 0.05%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
- Neurological disorders and treatments
Developmental Biology top 0.5%

Papers in

Molecular Biology 106
- RNA Research and Splicing 14
Neurology 78
- Parkinson's Disease Mechanisms and Treatments 48
- Amyotrophic Lateral Sclerosis Research 27
- Neurological diseases and metabolism 27

Co-authors: John C. van Swieten (36 shared papers)Ben A. Oostra (28 shared papers)Cornelia M. van Duijn (28 shared papers)Guido J. Breedveld (29 shared papers)Vincenzo Bonifati (17 shared papers)Marijke Joosse (11 shared papers)Patrizia Rizzu (19 shared papers)Alexis Brice (10 shared papers)
Journals: European Journal of Human Genetics (15 papers)Annals of Neurology (13 papers)The American Journal of Human Genetics (11 papers)PLoS ONE (10 papers)Movement Disorders (10 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Peter Heutink

233 papers receiving 17.3k citations

Peter Heutink's Hit Papers

5 papers align trajectories log scale

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies 2011 · 695 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2011 The Lancet
2011 Nature
2003 Science
1998 Nature Genetics
1994 Nature Genetics

Peers

Countries citing papers authored by Peter Heutink

Since Specialization

Citations

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

Fields of papers citing papers by Peter Heutink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Peter Heutink, 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 Peter Heutink Line = papers co-authored together Peter Heutink links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 241 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism Science ·Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Onno Schaap, Guido J. Breedveld, Elmar Krieger, Marieke Dekker, Ferdinando Squitieri, Pablo Ibáñez, Marijke Joosse, Jeroen W. van Dongen, Nicola Vanacore, John C. van Swieten, Alexis Brice, G. Meco, Cornelia M. van Duijn, Ben A. Oostra, Peter Heutink Hit paper breakdown →	2003	2313
2	Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1 Nature Genetics ·Kimberly A. McAllister, K.M. Grogg, David W. Johnson, Carol J. Gallione, Melanie A. Baldwin, Charles E. Jackson, E.A. Helmbold, Dorene S. Markel, Wendy McKinnon, J. Murrel, Mary Kay McCormick, M. A. Pericak‐Vance, Peter Heutink, Ben A. Oostra, T. Haitjema, C.J.J. Westerman, Mary Porteous, Alan E. Guttmacher, Michelle Letarte, Douglas A. Marchuk Hit paper breakdown →	1994	1234
3	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies The Lancet ·(unknown), Michael A. Nalls, Vincent Plagnol, Dena G Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, (unknown), María Martínez, John Hardy, Peter Heutink, Alexis Brice, Thomas Gasser, Andrew B. Singleton Hit paper breakdown →	2011	695
4	Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy Nature Genetics ·Bernard Brais, Jean‐Pierre Bouchard, Ya‐Gang Xie, Daniel Rochefort, Nathalie Chrétien, F.M.S. Tomé, Ronald G. Lafrentére, Johanna M. Rommens, Eichiro Uyama, O. Nohira, Segiu Blumen, Amos D. Korcyn, Peter Heutink, Jean Mathieu, André Duranceau, François Codère, Michel Fardeau, Guy A. Rouleau Hit paper breakdown →	1998	633
5	Somatic retrotransposition alters the genetic landscape of the human brain Nature ·J. Kenneth Baillie, Mark Barnett, Kyle R. Upton, Daniel J. Gerhardt, Todd Richmond, Fioravante De Sapio, Paul M. Brennan, Patrizia Rizzu, Sarah Smith, Mark Fell, Richard Talbot, Stefano Gustincich, (unknown), John S. Mattick, David Hume, Peter Heutink, Piero Carninci, Jeffrey A. Jeddeloh, Geoffrey J. Faulkner Hit paper breakdown →	2011	549
6	Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke New England Journal of Medicine ·Douglas B. Gould, F. Campbell Phalan, Saskia E. van Mil, John P. Sundberg, Katayoun Vahedi, Pascale Massin, Marie Germaine Bousser, Peter Heutink, Jeffrey H. Miner, Elisabeth Tournier‐Lasserve, Simon W. M. John	2006	437
7	Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly Science ·Douglas B. Gould, F. Campbell Phalan, Guido J. Breedveld, Saskia E. van Mil, Richard S. Smith, John C. Schimenti, Umberto Aguglia, Marjo S. van der Knaap, Peter Heutink, Simon W. M. John	2005	409
8	A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis Nature Genetics ·Omer T. Njajou, Norbert Vaessen, Marijke Joosse, Bianca Berghuis, Jeroen W.F. van Dongen, Martijn H. Breuning, Pieter J.L.M. Snijders, W. P. F. Rutten, Lodewijk A. Sandkuijl, Ben A. Oostra, Cornelia M. van Duijn, Peter Heutink	2001	403
9	Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly Proceedings of the National Academy of Sciences ·Laura A. Lettice, (unknown), Simon J. H. Heaney, Marijke J. van Baren, Herma C. van der Linde, Guido J. Breedveld, Marijke Joosse, Nurten Akarsu, Ben A. Oostra, Naoto Endo, Minoru Shibata, Mikio Suzuki, Eiichi Takahashi, Toshikatsu Shinka, Yutaka Nakahori, Dai Ayusawa, Kazuhiko Nakabayashi, Stephen W. Scherer, Peter Heutink, Robert E. Hill, Sumihare Noji	2002	372
10	High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands The American Journal of Human Genetics ·Patrizia Rizzu, John C. van Swieten, Marijke Joosse, Masato Hasegawa, Martijn Stevens, Aad Tibben, Martinus F. Niermeijer, Marcel Hillebrand, Rivka Ravid, Ben A. Oostra, Michel Goedert, Cornelia M. van Duijn, Peter Heutink	1999	372
11	DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism Neurological Sciences ·Vincenzo Bonifati, Patrizia Rizzu, Ferdinando Squitieri, Elmar Krieger, N. Vanacore, John C. van Swieten, Alexis Brice, Cornelia M. van Duijn, Ben A. Oostra, G. Meco, Peter Heutink	2003	337
12	Drosophila DJ-1 Mutants Are Selectively Sensitive to Environmental Toxins Associated with Parkinson’s Disease Current Biology ·Marc C. Meulener, Alexander J. Whitworth, Cecilia E. Armstrong‐Gold, Patrizia Rizzu, Peter Heutink, Paul D. Wes, Leo J. Pallanck, Nancy M. Bonini	2005	299
13	A Polymorphism in the Gene for IGF-I Diabetes ·Norbert Vaessen, Peter Heutink, J. A. M. J. L. Janssen, Jacqueline C.M. Witteman, Leon Testers, Albert Hofman, Steven W. J. Lamberts, Ben A. Oostra, Huibert A. P. Pols, Cornelia M. van Duijn	2001	298
14	PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36 The American Journal of Human Genetics ·Cornelia M. van Duijn, Marieke Dekker, Vincenzo Bonifati, Robert‐Jan H. Galjaard, Jeanine J. Houwing‐Duistermaat, Pieter J.L.M. Snijders, Leon Testers, Guido J. Breedveld, M.W.I.M. Horstink, L. Sandkuijl, John C. van Swieten, Ben A. Oostra, Peter Heutink	2001	293
15	Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of Tau American Journal Of Pathology ·Maria Grazia Spillantini, R. Anthony Crowther, Wouter Kamphorst, Peter Heutink, John C. van Swieten	1998	236
16	A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia The American Journal of Human Genetics ·John C. van Swieten, Esther Brusse, Bianca M. de Graaf, Elmar Krieger, Raoul van de Graaf, Inge de Koning, Anneke Maat‐Kievit, Peter A. J. Leegwater, Dennis Dooijes, Ben A. Oostra, Peter Heutink	2003	231
17	Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation Annals of Neurology ·Stephen Hague, Ekaterina Rogaeva, Dena G. Hernandez, Cindy Gulick, Amanda Singleton, Melissa Hanson, Janel Johnson, Roberto Weiser, Marisol Gallardo, Bernard Ravina, Katrina Gwinn, Anthony Crawley, Peter St George‐Hyslop, Anthony E. Lang, Peter Heutink, Vincenzo Bonifati, John Hardy, Andrew Singleton	2003	203
18	Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder Genomics ·Annemieke J.M.H. Verkerk, Carol A. Mathews, Marijke Joosse, Bert H.J. Eussen, Peter Heutink, Ben A. Oostra	2003	191
19	Phenotypic variation in hereditary frontotemporal dementia with tau mutations Annals of Neurology ·John C. van Swieten, M Stevens, Sonia M. Rosso, Patrizia Rizzu, Marijke Joosse, Inge de Koning, Wouter Kamphorst, Rivka Ravid, Maria Grazia Spillantini, Martinus F. Niermeijer, Peter Heutink	1999	190
20	Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's Annals of Neurology ·Ganqiang Liu, Brendon Boot, Joseph J. Locascio, Iris E. Jansen, Sophie Winder‐Rhodes, Shirley Eberly, Alexis Elbaz, Alexis Brice, Bernard Ravina, Jacobus J. van Hilten, Florence Cormier‐Dequaire, Jean‐Christophe Corvol, Roger A. Barker, Peter Heutink, Johan Marinus, Caroline H. Williams‐Gray, Clemens R. Scherzer	2016	186

About Peter Heutink

Peter Heutink is a scholar working on Molecular Biology, Neurology, Genetics, Physiology and Cellular and Molecular Neuroscience, having authored 241 papers that have together received 17.9k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (48 papers), Alzheimer's disease research and treatments (36 papers), Amyotrophic Lateral Sclerosis Research (27 papers), Neurological diseases and metabolism (27 papers), Genetic Associations and Epidemiology (22 papers), Congenital limb and hand anomalies (16 papers), Genetics and Neurodevelopmental Disorders (15 papers) and RNA Research and Splicing (14 papers). The work is most often cited by research in Neurology (6.3k citations), Neurology (2.3k citations), Developmental Biology (470 citations), Cellular and Molecular Neuroscience (3.7k citations) and Genetics (1.4k citations). Peter Heutink has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include John C. van Swieten, Ben A. Oostra, Cornelia M. van Duijn, Guido J. Breedveld, Vincenzo Bonifati, Marijke Joosse, Patrizia Rizzu, Alexis Brice, Ferdinando Squitieri and Elmar Krieger. Their work appears in journals such as European Journal of Human Genetics, Annals of Neurology, The American Journal of Human Genetics, PLoS ONE and Movement Disorders.

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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Peter Heutink

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In The Last Decade

Peter Heutink

Peter Heutink's Hit Papers

Peers

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Fields of papers citing papers by Peter Heutink

All Works

About Peter Heutink

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