M.P.A. Geurds

428 total citations
10 papers, 338 citations indexed

About

M.P.A. Geurds is a scholar working on Molecular Biology, Surgery and Rheumatology. According to data from OpenAlex, M.P.A. Geurds has authored 10 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Surgery and 3 papers in Rheumatology. Recurrent topics in M.P.A. Geurds's work include Folate and B Vitamins Research (3 papers), Cancer-related gene regulation (2 papers) and Kruppel-like factors research (2 papers). M.P.A. Geurds is often cited by papers focused on Folate and B Vitamins Research (3 papers), Cancer-related gene regulation (2 papers) and Kruppel-like factors research (2 papers). M.P.A. Geurds collaborates with scholars based in Netherlands, Germany and United States. M.P.A. Geurds's co-authors include Frans A. Hol, Edwin C.M. Mariman, Ben C.J. Hamel, Frans J.M. Trijbels, Sandra G. Heil, Henk J. Blom, Sansnee Chatkupt, William G. Johnson, Yin Yao Shugart and Rudi Balling and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

M.P.A. Geurds

10 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.P.A. Geurds Netherlands	8	162	160	105	100	78	10	338
Shaofang Shangguan China	12	165 1.0×	95 0.6×	109 1.0×	40 0.4×	94 1.2×	34	296
Gunnel Lundin Sweden	9	196 1.2×	72 0.5×	106 1.0×	34 0.3×	40 0.5×	12	384
Akiou Okumura Japan	10	41 0.3×	56 0.3×	41 0.4×	92 0.9×	50 0.6×	38	312
Émilie Lemieux‐Blanchard Canada	7	211 1.3×	216 1.4×	139 1.3×	20 0.2×	31 0.4×	17	457
Duccio Lombardi Italy	6	234 1.4×	16 0.1×	27 0.3×	56 0.6×	47 0.6×	15	395
Mabel Yau United States	11	239 1.5×	17 0.1×	145 1.4×	30 0.3×	124 1.6×	36	396
İbrahim Keser Türkiye	11	108 0.7×	26 0.2×	35 0.3×	27 0.3×	56 0.7×	32	291
D Zemková Czechia	13	95 0.6×	26 0.2×	37 0.4×	23 0.2×	145 1.9×	32	356
Wiedemann Hr	7	130 0.8×	37 0.2×	65 0.6×	35 0.3×	172 2.2×	42	316
Intza Garin Spain	17	476 2.9×	16 0.1×	114 1.1×	91 0.9×	506 6.5×	32	638

Countries citing papers authored by M.P.A. Geurds

Since Specialization

Citations

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

Fields of papers citing papers by M.P.A. Geurds

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.P.A. Geurds

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

All Works

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10 of 10 papers shown

Silahtaroglu, Asli, Frans A. Hol, Martin Erdel, et al.. (1999). Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. European Journal of Human Genetics. 7(1). 68–76. 16 indexed citations

Hol, Frans A., M.P.A. Geurds, Cor W. R. J. Cremers, Ben C.J. Hamel, & Edwin C.M. Mariman. (1998). Identification of two PAX3 mutations causing waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X). Human Mutation. 11(S1). S145–S147. 7 indexed citations

Hol, Frans A., M.P.A. Geurds, Sandra G. Heil, et al.. (1998). Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate‐dehydrogenase, methenyltetrahydrofolate‐cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects. Clinical Genetics. 53(2). 119–125. 127 indexed citations

Hol, Frans A., M.P.A. Geurds, Sansnee Chatkupt, et al.. (1996). PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.. Journal of Medical Genetics. 33(8). 655–660. 52 indexed citations

Hol, Frans A., et al.. (1995). Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family. Human Genetics. 95(6). 687–90. 21 indexed citations

Kok, Yvette J.M. de, M.P.A. Geurds, Erik A. Sistermans, et al.. (1995). Production of native creatine kinase B in insect cells using a baculovirus expression vector. Molecular and Cellular Biochemistry. 143(1). 59–65. 6 indexed citations

Hol, Frans A., Ben C.J. Hamel, M.P.A. Geurds, et al.. (1995). A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.. Journal of Medical Genetics. 32(1). 52–56. 44 indexed citations

Chatkupt, Sansnee, Frans A. Hol, Yin Yao Shugart, et al.. (1995). Absence of linkage between familial neural tube defects and PAX3 gene.. Journal of Medical Genetics. 32(3). 200–204. 25 indexed citations

Hol, Frans A., M.P.A. Geurds, O Jensson, et al.. (1994). Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family. Human Genetics. 93(4). 452–6. 9 indexed citations

10.

Hol, Frans A., M.P.A. Geurds, Ben C.J. Hamel, & Edwin C.M. Mariman. (1992). Improving the polymorphism content of the 3′ UTR of the human IGF2R gene. Human Molecular Genetics. 1(5). 347–347. 31 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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