Jan Osinga

2.1k citations

34 papers · 1.5k · h-index 23

Impact in

Cancer Research top 10%
- Cancer Genomics and Diagnostics
Genetics top 5%
- Digestive system and related health

Papers in

Molecular Biology 19
- RNA Research and Splicing 5
- RNA modifications and cancer 5
- Epigenetics and DNA Methylation 3
Surgery 11
- Congenital gastrointestinal and neural anomalies 10

Co-authors: Charles H.C.M. Buys (19 shared papers)Robert M.W. Hofstra (18 shared papers)Klaas Kok (5 shared papers)B. Carritt (3 shared papers)Pieter E. Postmus (3 shared papers)Anneke Y. van der Veen (4 shared papers)Annemarie H. van der Hout (3 shared papers)Henk H. Berendsen (3 shared papers)
Journals: Human Genetics (3 papers)The American Journal of Human Genetics (3 papers)Genes Chromosomes and Cancer (3 papers)Gastroenterology (2 papers)European Journal of Human Genetics (2 papers)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Jan Osinga

34 papers receiving 1.4k citations

Peers

Countries citing papers authored by Jan Osinga

Since Specialization

Citations

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

Fields of papers citing papers by Jan Osinga

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jan Osinga, 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 Jan Osinga Line = papers co-authored together Jan Osinga 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 34 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer Nature ·Klaas Kok, Jan Osinga, B. Carritt, Mary B. Davis, Annemarie H. van der Hout, Anneke Y. van der Veen, Rudy M. Landsvater, Lou F. M. H. de Leij, Henk H. Berendsen, Pieter E. Postmus, Sibrand Poppema, Charles H.C.M. Buys	1987	351
2	Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems The American Journal of Human Genetics ·Alice S. Brooks, Aida M. Bertoli‐Avella, Grzegorz Burzynski, Guido J. Breedveld, Jan Osinga, Ludolf G. Boven, Jane A. Hurst, Grazia M.S. Mancini, Maarten H. Lequin, I.F.M. de Coo, Ivana Matera, Esther de Graaff, Carel Meijers, Patrick J. Willems, Dick Tibboel, Ben A. Oostra, Robert M.W. Hofstra	2005	106
3	MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis Genes Chromosomes and Cancer ·Ying Wu, Minna Nyström, Jan Osinga, Maaike W.G. Looman, Païvi Peltomäki, Lauri A. Aaltonen, Albert de la Chapelle, Robert M.W. Hofstra, Charles H.C.M. Buys	1997	104
4	Abundance of protein-bound sulfhydryl and bisulfide groups at chromosomal nucleolus organizing regions Chromosoma ·Charles H.C.M. Buys, Jan Osinga	1980	100
5	RET-Familial Medullary Thyroid Carcinoma Mutants Y791F and S891A Activate a Src/JAK/STAT3 Pathway, Independent of Glial Cell Line–Derived Neurotrophic Factor Cancer Research ·Iván Plaza-Menacho, Roelof Koster, Almer M. van der Sloot, Wim J. Quax, Jan Osinga, Tineke van der Sluis, Harry Hollema, Grzegorz Burzynski, Oliver Gimm, Charles H.C.M. Buys, Bart J. L. Eggen, Robert M.W. Hofstra	2005	71
6	The Effects of Four Different Tyrosine Kinase Inhibitors on Medullary and Papillary Thyroid Cancer Cells The Journal of Clinical Endocrinology & Metabolism ·Hans H G Verbeek, Maria M. Alves, Jan‐Willem B. de Groot, Jan Osinga, John Th. M. Plukker, Thera P. Links, Robert M.W. Hofstra	2011	68
7	Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene Journal of the American College of Cardiology ·J. Peter van Tintelen, René A. Tio, Wilhelmina S. Kerstjens‐Frederikse, Jop H. van Berlo, Ludolf G. Boven, Albert J.H. Suurmeijer, Stefan J. White, Johan T. den Dunnen, Gerard J. te Meerman, Yvonne J. Vos, Annemarie H. van der Hout, Jan Osinga, Maarten P. van den Berg, Dirk J. van Veldhuisen, Charles H.C.M. Buys, Robert M.W. Hofstra, Yigal M. Pinto	2007	68
8	Selective staining of the same set of nucleolar phosphoproteins by silver and Giemsa Chromosoma ·Charles H.C.M. Buys, Jan Osinga	1984	60
9	Mutations in Hirschsprung Disease: When Does a Mutation Contribute to the Phenotype European Journal of Human Genetics ·Robert M.W. Hofstra, Jan Osinga, Charles H.C.M. Buys	1997	50
10	Identifying Candidate Hirschsprung Disease–Associated RET Variants The American Journal of Human Genetics ·Grzegorz Burzynski, Ilja M. Nolte, Agnes Bronda, Krista K. Bos, Jan Osinga, Iván Plaza-Menacho, Bas Twigt, Saskia M. Maas, Alice S. Brooks, B.G.M. Joke Verheij, H.C.M. Charles Buys, Robert M.W. Hofstra	2005	44
11	A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome) Journal of Medical Genetics ·AS Brooks, M.H. Breuning, Jan Osinga, J.J. Vd Smagt, C E Catsman, Chcm Buys, Carel Meijers, Robert M.W. Hofstra	1999	41
12	Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2 European Journal of Human Genetics ·Grzegorz Burzynski, Ilja M. Nolte, Jan Osinga, Isabella Ceccherini, Bas Twigt, Saskia M. Maas, Alice Brooks, Joanne Verheij, Iván Plaza-Menacho, Charles H.C.M. Buys, Robert M.W. Hofstra	2004	36
13	ABCD syndrome is caused by a homozygous mutation in the EDNRB gene American Journal of Medical Genetics ·Joanne Verheij, Jürgen Kunze, Jan Osinga, Anthonie J. van Essen, Robert M.W. Hofstra	2002	34
14	Variants in RET Associated With Hirschsprung's Disease Affect Binding of Transcription Factors and Gene Expression Gastroenterology ·Yunia Sribudiani, Marco Metzger, Jan Osinga, Amanda Rey, Alan J. Burns, Nikhil Thapar, Robert M.W. Hofstra	2010	33
15	KBP interacts with SCG10, linking Goldberg–Shprintzen syndrome to microtubule dynamics and neuronal differentiation Human Molecular Genetics ·Maria M. Alves, Grzegorz Burzynski, Jean‐Marie Delalande, Jan Osinga, Annemieke van der Goot, Amalia M. Dolga, Esther de Graaff, Alice S. Brooks, Marco Metzger, Ulrich Eisel, Iain T. Shepherd, Bart J. L. Eggen, Robert M.W. Hofstra	2010	32
16	A Rare Haplotype of the RET Proto-Oncogene Is a Risk-Modifying Allele in Hirschsprung Disease The American Journal of Human Genetics ·Paola Griseri, Bárbara Pesce, Giovanna Patrone, Jan Osinga, Francesca Puppo, Monica Sancandi, Robert M.W. Hofstra, G. Cara Romeo, Roberto Ravazzolo, Marcella Devoto, Isabella Ceccherini	2002	30
17	Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome Gene ·Jan J.J. Aalberts, J. Peter van Tintelen, Lilian J. Meijboom, A. H. Polko, Jan D.H. Jongbloed, Henriëtte van der Wal, Gerard Pals, Jan Osinga, Janneke Timmermans, Julie De Backer, Marian K. Bakker, Dirk J. van Veldhuisen, Robert M.W. Hofstra, Barbara J.M. Mulder, Maarten P. van den Berg	2013	27
18	MUTYH and the mismatch repair system: partners in crime? Human Genetics ·Renée C. Niessen, Rolf H. Sijmons, Jianghua Ou, Sandra Olthof, Jan Osinga, Marjolijn J. L. Ligtenberg, Frans B.L. Hogervorst, Marjan M. Weiss, Carli M.J. Tops, Frederik J. Hes, Geertruida H. de Bock, Charles H.C.M. Buys, Jan H. Kleibeuker, Robert M.W. Hofstra	2006	26
19	Loss of heterozygosity for a chromosome 3 sequence presumably at 3p21 in small cell lung cancer Cancer Genetics and Cytogenetics ·Hans Mooibroek, Jan Osinga, Pieter E. Postmus, B. Carritt, Charles H.C.M. Buys	1987	26
20	Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease Gastroenterology ·Yunia Sribudiani, Rajendra Chauhan, Maria M. Alves, Lucy Petrova, Erwin Brosens, Colin Harrison, Tara D. Wabbersen, Bianca M. de Graaf, Tim Rügenbrink, Grzegorz Burzynski, Rutger W. W. Brouwer, Wilfred F. J. van IJcken, Saskia M. Maas, Annelies de Klein, Jan Osinga, Bart J. L. Eggen, Alan J. Burns, Alice S. Brooks, Iain T. Shepherd, Robert M.W. Hofstra	2018	26

About Jan Osinga

Jan Osinga is a scholar working on Molecular Biology, Surgery, Oncology, Cancer Research and Genetics, having authored 34 papers that have together received 1.5k indexed citations. Recurring topics across this work include Congenital gastrointestinal and neural anomalies (10 papers), RNA Research and Splicing (5 papers), RNA modifications and cancer (5 papers), Lung Cancer Research Studies (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Cancer Genomics and Diagnostics (4 papers), Genetic factors in colorectal cancer (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Cancer Research (288 citations), Genetics (365 citations), Oncology (342 citations), Pathology and Forensic Medicine (225 citations) and Molecular Biology (754 citations). Jan Osinga has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Charles H.C.M. Buys, Robert M.W. Hofstra, Klaas Kok, B. Carritt, Pieter E. Postmus, Anneke Y. van der Veen, Annemarie H. van der Hout, Henk H. Berendsen, Sibrand Poppema and Mary B. Davis. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Genes Chromosomes and Cancer, Gastroenterology and European Journal of Human Genetics.

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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Jan Osinga

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