P. Mollevanger

627 citations

19 papers · 428 · h-index 13

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
Hematology
- Acute Myeloid Leukemia Research

Papers in

Genetics 12
- Genomic variations and chromosomal abnormalities 10
- Chronic Lymphocytic Leukemia Research 3
Molecular Biology 9

Co-authors: J.W. Wessels (4 shared papers)Vincent T.H.B.M. Smit (4 shared papers)G.C. Beverstock (4 shared papers)Peter Devilee (3 shared papers)Hanneke C. Kluin‐Nelemans (3 shared papers)JH Falkenburg (3 shared papers)Leendert H. J. Looijenga (2 shared papers)J. Wolter Oosterhuis (2 shared papers)
Journals: Blood (4 papers)Genomics (2 papers)Journal of Medical Genetics (2 papers)Cytogenetic and Genome Research (2 papers)Fertility and Sterility (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

P. Mollevanger

19 papers receiving 419 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	Localization and polymorphism of a chromosome 12-specific α satellite DNA sequence Cytogenetic and Genome Research ·Leendert H. J. Looijenga, Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, J. Wolter Oosterhuis, C.J. Cornelisse, Peter Devilee	1990	68
2	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	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	42
4	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
5	Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes Cytogenetic and Genome Research ·Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, Peter I. Schrier, Anton K. Raap, G.C. Beverstock, Cees J. Cornelisse	1990	31
6	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	29
7	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
8	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	28
9	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	27
10	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
11	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
12	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	12
13	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
14	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	12
15	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
16	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	10
17	A girl with 71,XXXXY karyotype Clinical Genetics ·P. D. Maaswinksl‐Mooij, P. van Zwieten, P. Mollevanger, Ellen Van Noort, G.C. Beverstock	1992	3
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	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

About P. Mollevanger

P. Mollevanger is a scholar working on Genetics, Molecular Biology, Plant Science, Hematology and Genetics, having authored 19 papers that have together received 428 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), Lymphoma Diagnosis and Treatment (2 papers), Chronic Myeloid Leukemia Treatments (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). The work is most often cited by research in Genetics (189 citations), Hematology (65 citations), Genetics (51 citations), Pathology and Forensic Medicine (56 citations) and Pediatrics, Perinatology and Child Health (59 citations). P. Mollevanger has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include J.W. Wessels, Vincent T.H.B.M. Smit, G.C. Beverstock, Peter Devilee, Hanneke C. Kluin‐Nelemans, JH Falkenburg, Leendert H. J. Looijenga, J. Wolter Oosterhuis, Geoffrey C. Beverstock and C.J. Cornelisse. Their work appears in journals such as Blood, Genomics, Journal of Medical Genetics, Cytogenetic and Genome Research and Fertility and Sterility.

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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