P. Mollevanger

627 total citations
19 papers, 428 citations indexed

About

P. Mollevanger is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, P. Mollevanger has authored 19 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in P. Mollevanger's work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers) and Acute Myeloid Leukemia Research (3 papers). P. Mollevanger is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (8 papers) and Acute Myeloid Leukemia Research (3 papers). P. Mollevanger collaborates with scholars based in Netherlands, United States and Germany. P. Mollevanger's co-authors include Vincent T.H.B.M. Smit, J.W. Wessels, 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 and has published in prestigious journals such as Blood, Fertility and Sterility and Genomics.

In The Last Decade

P. Mollevanger

19 papers receiving 419 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
P. Mollevanger Netherlands	13	196	189	95	65	59	19	428
J.W. Wessels Netherlands	8	216 1.1×	173 0.9×	118 1.2×	173 2.7×	39 0.7×	10	445
Renée Bernstein South Africa	13	241 1.2×	195 1.0×	49 0.5×	163 2.5×	64 1.1×	26	466
Shunsuke Kimura Japan	13	203 1.0×	144 0.8×	31 0.3×	95 1.5×	67 1.1×	40	476
M. L. Kwee Netherlands	13	426 2.2×	320 1.7×	57 0.6×	55 0.8×	91 1.5×	24	640
Christine R. Bryke United States	13	268 1.4×	229 1.2×	45 0.5×	64 1.0×	42 0.7×	31	529
Elena Gaber Israel	13	194 1.0×	143 0.8×	39 0.4×	65 1.0×	32 0.5×	22	449
Sparkes Rs United States	11	143 0.7×	132 0.7×	42 0.4×	122 1.9×	72 1.2×	30	382
Claudia Dellavecchia Italy	9	153 0.8×	220 1.2×	87 0.9×	59 0.9×	93 1.6×	11	408
Peter C. Verlander United States	14	695 3.5×	255 1.3×	82 0.9×	100 1.5×	45 0.8×	18	921
Anne Marie Ottesen Denmark	11	371 1.9×	390 2.1×	70 0.7×	17 0.3×	71 1.2×	15	733

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-authorship network of co-authors of P. Mollevanger

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

All Works

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19 of 19 papers shown

Bezrookove, Vladimir, P. Mollevanger, Jacques J. P. van de Kamp, et al.. (2003). 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. 122A(2). 168–173. 10 indexed citations

Nijmeijer, Bart, et al.. (2001). Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice. Experimental Hematology. 29(3). 322–329. 42 indexed citations

Beverstock, Geoffrey C., et al.. (1999). Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis. Cancer Genetics and Cytogenetics. 115(1). 11–18. 11 indexed citations

Zelderen‐Bhola, Shama L. van, et al.. (1998). Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma. Cancer Genetics and Cytogenetics. 105(2). 109–112. 12 indexed citations

Kant, Sarina G., Arie van Haeringen, Ingrid Stec, et al.. (1997). 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. 34(7). 569–572. 12 indexed citations

Beverstock, Geoffrey C., Paul H. E. Meijer, Daan ten Bokkel Huinink, et al.. (1996). A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia. Cancer Genetics and Cytogenetics. 89(2). 132–135. 12 indexed citations

Horsthemke, Bernhard, Anneke Maat‐Kievit, A. van den Ouweland, et al.. (1996). Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.. Journal of Medical Genetics. 33(10). 848–851. 28 indexed citations

Kluin‐Nelemans, Hanneke C., G.C. Beverstock, P. Mollevanger, et al.. (1994). Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen. Blood. 84(9). 3134–3141. 50 indexed citations

Kluin‐Nelemans, Hanneke C., et al.. (1994). Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen. Blood. 84(9). 3134–3141. 2 indexed citations

10.

Looijenga, Leendert H. J., J. Wolter Oosterhuis, Vincent T.H.B.M. Smit, et al.. (1992). 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. 13(4). 1125–1132. 16 indexed citations

11.

Mollevanger, P., et al.. (1992). A girl with 71,XXXXY karyotype. Clinical Genetics. 41(2). 96–99. 3 indexed citations

12.

Dauwerse, Johannes G., Martin C. Wapenaar, Eric J. Meershoek, et al.. (1991). 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. 11(4). 1079–1087. 32 indexed citations

13.

Veneman, Thiemo, Geoffrey C. Beverstock, N. Exalto, & P. Mollevanger. (1991). Premature menopause because of an inherited deletion in the long arm of the X-chromosome. Fertility and Sterility. 55(3). 631–633. 29 indexed citations

14.

Smit, Vincent T.H.B.M., J.W. Wessels, P. Mollevanger, et al.. (1991). 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. 3(4). 239–248. 29 indexed citations

15.

Wessels, J., et al.. (1991). Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia. Blood. 77(7). 1555–1559. 27 indexed citations

16.

Mollevanger, P., et al.. (1991). Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia. Blood. 77(7). 1555–1559. 2 indexed citations

17.

Looijenga, Leendert H. J., Vincent T.H.B.M. Smit, J.W. Wessels, et al.. (1990). Localization and polymorphism of a chromosome 12-specific α satellite DNA sequence. Cytogenetic and Genome Research. 53(4). 216–218. 68 indexed citations

18.

Smit, Vincent T.H.B.M., J.W. Wessels, P. Mollevanger, et al.. (1990). Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes. Cytogenetic and Genome Research. 54(1-2). 20–23. 31 indexed citations

19.

Beverstock, Geoffrey C., et al.. (1990). Trisomy 13 and myelodysplastic syndrome. Cancer Genetics and Cytogenetics. 48(2). 179–182. 12 indexed citations

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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