P. Mollevanger

629 citations

19 papers · 391 · h-index 13

Impact in

Genetics
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
- Genetic Syndromes and Imprinting
Hematology
- Acute Myeloid Leukemia Research

Papers in

Genetics 12
- Genomic variations and chromosomal abnormalities 10
- Chronic Lymphocytic Leukemia Research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
Molecular Biology 8

Co-authors: Geoffrey C. Beverstock (4 shared papers)JH Falkenburg (3 shared papers)Hanneke C. Kluin‐Nelemans (3 shared papers)G.C. Beverstock (4 shared papers)N. Exalto (1 shared paper)Thiemo Veneman (1 shared paper)Shama L. van Zelderen‐Bhola (2 shared papers)R. Willemze (2 shared papers)
Journals: Blood (4 papers)Genomics (2 papers)Journal of Medical Genetics (2 papers)Fertility and Sterility (1 paper)Experimental Hematology (1 paper)
Partner nations: Netherlands Germany United States

In The Last Decade

P. Mollevanger

18 papers receiving 350 citations

Peers

Countries citing papers authored by P. Mollevanger

Since Specialization

Citations

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

Fields of papers citing papers by P. Mollevanger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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19 of 19 papers shown

#	Work
1	Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen Blood ·Hanneke C. Kluin‐Nelemans, G.C. Beverstock, P. Mollevanger, HW Wessels, E Hoogendoorn, R. Willemze, JH Falkenburg	1994	54
2	Premature menopause because of an inherited deletion in the long arm of the X-chromosome Fertility and Sterility ·Thiemo Veneman, Geoffrey C. Beverstock, N. Exalto, P. Mollevanger	1991	50
3	Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice Experimental Hematology ·Bart Nijmeijer, P. Mollevanger, Shama L. van Zelderen‐Bhola, Hanneke C. Kluin‐Nelemans, Roel Willemze, JH Falkenburg	2001	45
4	Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome. Journal of Medical Genetics ·Bernhard Horsthemke, Anneke Maat‐Kievit, Eva Sleegers, A. van den Ouweland, Karin Buiting, Christina Lich, P. Mollevanger, G.C. Beverstock, Gabriele Gillessen‐Kaesbach, Gesa Schwanitz	1996	45
5	Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library Genomics ·M. Driesen, Johannes G. Dauwerse, Martin C. Wapenaar, Eric J. Meershoek, P. Mollevanger, K.L. Chen, Kenneth H. Fischbeck, G.J.B. van Ommen	1991	32
6	Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome‐specific libraries and cosmid probes Genes Chromosomes and Cancer ·Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, Johannes G. Dauwerse, M. van Vliet, G.C. Beverstock, M.H. Breuning, Peter Devilee, Anton K. Raap, Cees J. Cornelisse	1991	29
7	Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia Blood ·J. Wessels, P. Mollevanger, JG Dauwerse, F. H. M. Cluitmans, M.H. Breuning, G.C. Beverstock	1991	29
8	Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma Cancer Genetics and Cytogenetics ·Shama L. van Zelderen‐Bhola, Judith V.M.G. Bovée, Hans W. Wessels, P. Mollevanger, Jeroen V. Nijhuis, Jaap D. H. van Eendenburg, A. H. M. Taminiau, Pancras C.W. Hogendoorn	1998	16
9	Alpha satellite DNAs on chromosomes 10 and 12 are both members of the dimeric suprachromosomal subfamily, but display little identity at the nucleotide sequence level Genomics ·Leendert H. J. Looijenga, J. Wolter Oosterhuis, Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, Peter Devilee	1992	16
10	Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3. Journal of Medical Genetics ·Sarina G. Kant, Arie van Haeringen, E Bakker, Ingrid Stec, Dian Donnai, P. Mollevanger, G.C. Beverstock, M.C. Lindeman-Kusse, G J van Ommen	1997	15
11	Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature American Journal of Medical Genetics Part A ·Geoff C. Beverstock, Vladimir Bezrookove, P. Mollevanger, Jacques J. P. van de Kamp, P. Pearson, J.M. Kouwenberg, Carla Rosenberg	2003	12
12	Trisomy 13 and myelodysplastic syndrome Cancer Genetics and Cytogenetics ·Geoffrey C. Beverstock, J. E. Ploem, H. Wessels, D. van der Keur, P. Mollevanger	1990	12
13	A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia Cancer Genetics and Cytogenetics ·Geoffrey C. Beverstock, Paul H. E. Meijer, Daan ten Bokkel Huinink, Hans Pruijt, G. J. den Ottolander, Hans W. Wessels, P. Mollevanger	1996	12
14	Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis Cancer Genetics and Cytogenetics ·Geoffrey C. Beverstock, P. Mollevanger, Marjolein Baaij, Jeanette Lind, Liesbeth van Ieperen, Margot M. Bartelings, K. Teunissen, Helen Brandenburg, Diane Van Opstal, Frans Los	1999	11
15	A girl with 71,XXXXY karyotype Clinical Genetics ·P. D. Maaswinksl‐Mooij, P. van Zwieten, P. Mollevanger, Ellen Van Noort, G.C. Beverstock	1992	5
16	Localization and polymorphism of a chromosome 12-specific α satellite DNA sequence Cytogenetics and Cell Genetics ·Leendert H. J. Looijenga, Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, J. Wolter Oosterhuis, C.J. Cornelisse, Peter Devilee	2008	4
17	Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia Blood ·JW Wessels, P. Mollevanger, JG Dauwerse, F. H. M. Cluitmans, MH Breuning, G.C. Beverstock	1991	2
18	Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen Blood ·Hanneke C. Kluin‐Nelemans, GC Beverstock, P. Mollevanger, HW Wessels, E Hoogendoorn, R. Willemze, JH Falkenburg	1994	2
19	Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes Cytogenetics and Cell Genetics ·Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, Peter I. Schrier, Anton K. Raap, G.C. Beverstock, Cees J. Cornelisse	2008	0

About P. Mollevanger

P. Mollevanger is a scholar working on Genetics, Molecular Biology, Plant Science, Genetics and Pathology and Forensic Medicine, having authored 19 papers that have together received 391 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers), Acute Myeloid Leukemia Research (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Acute Lymphoblastic Leukemia research (2 papers) and Lymphoma Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (164 citations), Hematology (57 citations), Genetics (47 citations), Pediatrics, Perinatology and Child Health (53 citations) and Developmental Biology (6 citations). P. Mollevanger has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Geoffrey C. Beverstock, JH Falkenburg, Hanneke C. Kluin‐Nelemans, G.C. Beverstock, N. Exalto, Thiemo Veneman, Shama L. van Zelderen‐Bhola, R. Willemze, G.C. Beverstock and M.H. Breuning. Their work appears in journals such as Blood, Genomics, Journal of Medical Genetics, Fertility and Sterility and Experimental Hematology.

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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