Jan Maarten Cobben

625 total citations
18 papers, 331 citations indexed

About

Jan Maarten Cobben is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Jan Maarten Cobben has authored 18 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in Jan Maarten Cobben's work include Prenatal Screening and Diagnostics (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Prenatal Substance Exposure Effects (3 papers). Jan Maarten Cobben is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Prenatal Substance Exposure Effects (3 papers). Jan Maarten Cobben collaborates with scholars based in Netherlands, United States and United Kingdom. Jan Maarten Cobben's co-authors include Raoul C. M. Hennekam, Lambert Schuwirth, Allard C. van der Wal, Sally‐Ann B. Clur, Leonie A. Menke, Catia M. Bilardo, Henny H. Lemmink, Lidewij Henneman, Albert Scherpbier and Leo P. ten Kate and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Fertility and Sterility.

In The Last Decade

Jan Maarten Cobben

18 papers receiving 320 citations

Peers

Countries citing papers authored by Jan Maarten Cobben

Since Specialization

Citations

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

Fields of papers citing papers by Jan Maarten Cobben

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan Maarten Cobben. 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 Jan Maarten Cobben. The network helps show where Jan Maarten Cobben may publish in the future.

Co-authorship network of co-authors of Jan Maarten Cobben

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Maarten Cobben. A scholar is included among the top collaborators of Jan Maarten Cobben 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 Jan Maarten Cobben. Jan Maarten Cobben is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Expression Quantitative Trait Methylation Analysis Identifies Whole Blood Molecular Footprint in Fetal Alcohol Spectrum Disorder (FASD) 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Adri N. Mul, (unknown), Andrew Y. F. Li Yim, Jan Maarten Cobben, Jacek Nikliński, (unknown), Robert Śmigiel, Marcel M. A. M. Mannens, Peter Henneman	5
2	DNA Methylation Abundantly Associates with Fetal Alcohol Spectrum Disorder and its Subphenotypes 2019 ·Epigenomics ·Jan Maarten Cobben, (unknown), Andrea Venema, Adri N. Mul, Abeltje M. Polstra, Alex V. Postma, Robert Śmigiel, Karolina Pesz, Jacek Nikliński, (unknown), Peter Henneman, Marcel M. A. M. Mannens	26
3	Mutations in Histone Acetylase Modifier BRPF1 Cause an Autosomal-Dominant Form of Intellectual Disability with Associated Ptosis 2016 ·The American Journal of Human Genetics ·Francesca Mattioli, Élise Schaefer, Alex Magee, Paul R. Mark, Grazia M.S. Mancini, Klaus Dieterich, Gretchen Von Allmen, Mariëlle Alders, Charles Coutton, Marjon van Slegtenhorst, Gaëlle Vieville, Marc Engelen, Jan Maarten Cobben, Jane Juusola, Aurora Pujol, Jean‐Louis Mandel, Amélie Piton	42
4	Trisomy 4 mosaicism: Delineation of the phenotype 2016 ·American Journal of Medical Genetics Part A ·Arjan Bouman, Anne-Marie Van Der Kevie-Kersemaekers, Karin Huijsdens–van Amsterdam, (unknown), (unknown), Fleur Vansenne, Jan Maarten Cobben	2
5	Etiology and pathogenesis of robin sequence in a large Dutch cohort 2015 ·American Journal of Medical Genetics Part A ·Hanneke Basart, Emma C. Paes, Saskia M. Maas, Marie‐José H. van den Boogaard, Johanna M. van Hagen, Corstiaan C. Breugem, Jan Maarten Cobben, J. Peter W. Don Griot, Augusta M.A. Lachmeijer, Klaske D. Lichtenbelt, (unknown), Chantal M.A.M. van der Horst, Raoul C. M. Hennekam	29
6	Congenital thrombocytopenia in a neonate with an interstitial microdeletion of 3q26.2q26.31 2015 ·American Journal of Medical Genetics Part A ·Arjan Bouman, (unknown), Stefan Gröschel, Claudia Erpelinck-Verschueren, Mathijs A. Sanders, Ruud Delwel, Taco W. Kuijpers, Jan Maarten Cobben	13
7	Complete and partial XYLT1 deletion in a patient with neonatal short limb skeletal dysplasia 2015 ·American Journal of Medical Genetics Part A ·Silvana van Koningsbruggen, Hennie Knoester, Roel Bakx, Olaf R.F. Mook, (unknown), Jan Maarten Cobben	12
8	Diagnostic outcomes of 27 children referred by pediatricians to a genetics clinic in the Netherlands with suspicion of fetal alcohol spectrum disorders 2013 ·American Journal of Medical Genetics Part A ·(unknown), Mieke M. van Haelst, Grazia M.S. Mancini, Connie Schrander‐Stumpel, (unknown), Raoul C. M. Hennekam, Jan Maarten Cobben	12
9	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
10	Morphologic abnormalities in 2-year-old children born after in vitro fertilization/intracytoplasmic sperm injection with preimplantation genetic screening: follow-up of a randomized controlled trial 2012 ·Fertility and Sterility ·(unknown), (unknown), Jack J. Middelburg, Jan Maarten Cobben, Sebastiaan Mastenbroek, (unknown), Johanna H. van der Lee, Mijna Hadders‐Algra, Arend F. Bos, Joke H. Kok	10
11	Beare-Stevenson Syndrome: Two Dutch Patients With Cerebral Abnormalities 2011 ·Pediatric Neurology ·Daniela Q.C.M. Barge‐Schaapveld, Alice S. Brooks, Maarten H. Lequin, (unknown), R. Jeroen Vermeulen, Jan Maarten Cobben	10
12	Ectrodactyly with fibular aplasia: A separate entity? 2008 ·European Journal of Medical Genetics ·Leonie A. Menke, Emilia K. Bijlsma, Anthonie J. van Essen, Marie‐José H. van den Boogaard, Rick R. van Rijn, Jan Maarten Cobben	3
13	Congenital heart defects in spinal muscular atrophy type I: A clinical report of two siblings and a review of the literature 2008 ·American Journal of Medical Genetics Part A ·Leonie A. Menke, Bwee Tien Poll‐The, Sally‐Ann B. Clur, Catia M. Bilardo, Allard C. van der Wal, Henny H. Lemmink, Jan Maarten Cobben	39
14	DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands 2007 ·European Journal of Medical Genetics ·Hester Y. Kroes, (unknown), (unknown), Marcel Nelen, (unknown), D. Wittebol‐Post, Onno van Nieuwenhuizen, Grazia M.S. Mancini, Marjo S. van der Knaap, M. L. Kwee, Saskia M. Maas, Jan Maarten Cobben, (unknown), Dick Lindhout, Richard J. Sinke	27
15	Normal values for morphological abnormalities in school children 2006 ·American Journal of Medical Genetics Part A ·Johannes H. M. Merks, Mihriban Heval Özgen, (unknown), (unknown), Jan Maarten Cobben, Flora E. van Leeuwen, Raoul C. M. Hennekam	26
16	Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation 2005 ·Genetics in Medicine ·Marieke J.H. Baars, Albert Scherpbier, Lambert Schuwirth, Lidewij Henneman, Frits A. Beemer, Jan Maarten Cobben, Raoul C. M. Hennekam, (unknown), Martina C. Cornel, Leo P. ten Kate	56
17	Renal defects and limb deficiencies in 197 infants: Is it possible to define the “acrorenal syndrome”? 2004 ·American Journal of Medical Genetics Part A ·Hester Y. Kroes, Richard S. Olney, Aldo Rosano, Yecai Liu, Eduardo E. Castilla, Guido Cocchi, Catherine De Vigan, María Luisa Martínez‐Frías, Pierpaolo Mastroiacovo, Paul Merlob, Osvaldo M. Mutchinick, Annukka Ritvanen, Claude Stoll, Anthonie J. van Essen, Jan Maarten Cobben, Martina C. Cornel	8
18	DNA-studies in spinal muscular atrophy 1996 ·Data Archiving and Networked Services (DANS) ·Jan Maarten Cobben	2

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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