J. O. Van Hemel

1.8k citations

38 papers · 1.1k indexed · h-index 21

Genetics top 2%
Molecular Biology
Pediatrics, Perinatology and Child Health top 5%
Plant Science top 10%
Cognitive Neuroscience top 10%

Co-authors: H. J. Eussen Martinus F. Niermeijer E. S. Sachs M. G. J. Jahoda Eveline Wesby–van Swaay D. J. J. Halley Jan C. den Hollander Frans J. Los
Topics: Genomic variations and chromosomal abnormalities (19 papers)Prenatal Screening and Diagnostics (12 papers)Genetics and Neurodevelopmental Disorders (10 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Reproductive Medicine
Journals: The Lancet The Journal of Urology Human Reproduction
Partner nations: Netherlands Belgium Australia

In The Last Decade

J. O. Van Hemel

38 papers receiving 1.1k citations

Peers

Countries citing papers authored by J. O. Van Hemel

Since Specialization

Citations

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

Fields of papers citing papers by J. O. Van Hemel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. O. Van Hemel. 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 J. O. Van Hemel. The network helps show where J. O. Van Hemel may publish in the future.

Co-authorship network of co-authors of J. O. Van Hemel

This figure shows the co-authorship network connecting the top 25 collaborators of J. O. Van Hemel. A scholar is included among the top collaborators of J. O. Van Hemel 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 J. O. Van Hemel. J. O. Van Hemel 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	Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome 2001 ·American Journal of Medical Genetics ·Carine Wouters,(unknown),(unknown),(unknown),(unknown),(unknown),Berna Beverloo,Frank Visscher,J. O. Van Hemel	6
2	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) 1999 ·American Journal of Medical Genetics ·Bert B.A. de Vries,Bert H.J. Eussen,Otto P. van Diggelen,(unknown),(unknown),Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	1
3	Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) 1999 ·American Journal of Medical Genetics ·(unknown),Bert H.J. Eussen,Otto P. van Diggelen,(unknown),(unknown),Lutgarde Govaerts,Dick Lindhout,Carine Wouters,J. O. Van Hemel	12
4	Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection 1997 ·Human Reproduction ·Diane Van Opstal,Frans J. Los,(unknown),J. O. Van Hemel,A M van den Ouweland,H. Brandenburg,M.H.E.C. Pieters,Arie Verhoeff,M. Vermeer,Marc Dhont,Pieter In 'T Veld	115
5	Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection 1997 ·Human Reproduction ·Pieter In 'T Veld,R. F. A. Weber,Frans J. Los,Nicolette S. den Hollander,Marc Dhont,M.H.E.C. Pieters,J. O. Van Hemel	43
6	The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells 1996 ·American Journal of Medical Genetics ·Esther de Graaff,Bert de Vries,(unknown),J. O. Van Hemel,Serieta Mohkamsing,Ben A. Oostra,(unknown)	34
7	Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family. 1996 ·Journal of Medical Genetics ·(unknown),(unknown),Annelien Duits,(unknown),Rob Willemsen,J. O. Van Hemel,A M van den Ouweland,Martinus F. Niermeijer,B. A. Oostra,D. J. J. Halley	62
8	A chromosome 21‐specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei 1995 ·Prenatal Diagnosis ·Diane Van Opstal,J. O. Van Hemel,Bert H.J. Eussen,(unknown),Cardi van den Berg,Pieter In 'T Veld,Frans J. Los	8
9	DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR‐1 gene 1994 ·American Journal of Medical Genetics ·Ans M.W. van den Ouweland,Bert B.A. de Vries,(unknown),Wout H. Deelen,Esther de Graaff,J. O. Van Hemel,Ben A. Oostra,Martinus F. Niermeijer,Dicky Halley	43
10	Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. 1993 ·Journal of Medical Genetics ·Bert Ba de Vries,J. P. Fryns,Merlin G. Butler,(unknown),Eveline Wesby–van Swaay,J. O. Van Hemel,Ben A. Oostra,D. J. J. Halley,Martinus F. Niermeijer	73
11	Application of fluorescent in situ hybridization for ‘de novo’ anomalies in prenatal diagnosis 1993 ·Prenatal Diagnosis ·Diane Van Opstal,H. J. Eussen,J. O. Van Hemel,E. S. Sachs	12
12	Avoidance of emergency surgery in newborn infants with trisomy 18 1992 ·The Lancet ·(unknown),(unknown),Frans W.J. Hazebroek,Dick Tibboel,J.C. Molenaar,J. O. Van Hemel,Eveline Wesby–van Swaay	52
13	Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome 1992 ·Human Genetics ·J. O. Van Hemel,Bert Eussen,Eveline Wesby–van Swaay,B. A. Oostra	26
14	Limited size of the fragile X site shown by fluorescence in situ hybridization 1992 ·American Journal of Medical Genetics ·Annemieke J.M.H. Verkerk,Bert H.J. Eussen,J. O. Van Hemel,Ben A. Oostra	11
15	DNA analysis in patients with lissencephaly type I and other cortical dysplasias 1991 ·American Journal of Medical Genetics ·B. A. Oostra,J.F. de Rijk-van Andel,H. J. Eussen,J. O. Van Hemel,D. J. J. Halley,Martinus F. Niermeijer	5
16	Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27–q28 1991 ·American Journal of Medical Genetics ·B. A. Oostra,Daniëlle Majoor‐Krakauer,J. O. Van Hemel,Egbert Bakker,David F. Callen,Malgorzata Schmidt,Bernard A. van Oost	5
17	Clinical and Chromosome Studies of Three Patients with Smith‐Magenis Syndrome 1991 ·Developmental Medicine & Child Neurology ·J.F. de Rijk-van Andel,Coriene E. Catsman‐Berrevoets,J. O. Van Hemel,A.J.H. Hamers	25
18	Paracentric inversion inv(11) (q21q23) in the Netherlands 1990 ·Human Genetics ·K. Madan,M.H.E.C. Pieters,L. P. Kuyt,C. J. van Asperen,Jennie M. Pater,A.J.H. Hamers,(unknown),T. W. J. Hustinx,(unknown),J. O. Van Hemel,Dominique Smeets	11
19	The 5q‐ chromosome abnormality in haematological disorders:\|a collaborative study of 34 cases from the Netheralands 1982 ·British Journal of Haematology ·H. Kerkhofs,A Hagemeijer,C. H. W. Leeksma,J. Abels,(unknown),R. Somers,(unknown),(unknown),(unknown),J. O. Van Hemel,J. P. M. Geraedts	74
20	Ring chromosome 2: Clinical, chromosomal, and biochemical aspects 1982 ·Human Genetics ·M. Jansen,F. A. Beemer,Colin van der Heiden,J. O. Van Hemel,J. L. Van den Brande	16

About J. O. Van Hemel

J. O. Van Hemel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Urology, having authored 38 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). The work is most often cited by research in Genetics (809 citations), Pediatrics, Perinatology and Child Health (356 citations) and Reproductive Medicine (94 citations). J. O. Van Hemel has collaborated with scholars based in Netherlands, Belgium and Australia. Frequent co-authors include H. J. Eussen, Martinus F. Niermeijer, E. S. Sachs, M. G. J. Jahoda, Eveline Wesby–van Swaay, D. J. J. Halley, Jan C. den Hollander, Frans J. Los, Pieter In 'T Veld and M.H.E.C. Pieters. Their work appears in journals such as The Lancet, The Journal of Urology and Human Reproduction.

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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