G.J. te Meerman

412 total citations
15 papers, 326 citations indexed

About

G.J. te Meerman is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, G.J. te Meerman has authored 15 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in G.J. te Meerman's work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Associations and Epidemiology (2 papers) and CRISPR and Genetic Engineering (2 papers). G.J. te Meerman is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetic Associations and Epidemiology (2 papers) and CRISPR and Genetic Engineering (2 papers). G.J. te Meerman collaborates with scholars based in Netherlands, India and Germany. G.J. te Meerman's co-authors include Marian van der Meulen, Lodewijk A. Sandkuijl, Hans Scheffer, Ilja M. Nolte, Martina C. Cornel, C.H.C.M. Buys, Gert J. Ter Horst, Andrea Trentani, Johanna M. Beekman and Johan A. den Boer and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and European Journal of Cancer.

In The Last Decade

G.J. te Meerman

15 papers receiving 318 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G.J. te Meerman Netherlands	12	150	102	35	35	35	15	326
Peiyin Wang United States	7	161 1.1×	230 2.3×	10 0.3×	39 1.1×	42 1.2×	11	378
Shayne F. Andrew United States	13	133 0.9×	156 1.5×	44 1.3×	49 1.4×	157 4.5×	20	456
Victoria L. Turgeon United States	7	28 0.2×	207 2.0×	19 0.5×	101 2.9×	24 0.7×	11	468
Shinichi Yotsumoto Japan	13	62 0.4×	251 2.5×	23 0.7×	48 1.4×	42 1.2×	25	456
Anna L. Travelstead United States	16	143 1.0×	66 0.6×	84 2.4×	41 1.2×	67 1.9×	18	691
Joseph G. Eichen United States	6	154 1.0×	183 1.8×	18 0.5×	121 3.5×	28 0.8×	7	637
Leah W. Burke United States	13	247 1.6×	182 1.8×	49 1.4×	34 1.0×	31 0.9×	22	552
Hylke M. Blauw Netherlands	11	140 0.9×	220 2.2×	9 0.3×	41 1.2×	16 0.5×	13	680
Teresa Neuhann Germany	14	189 1.3×	215 2.1×	32 0.9×	43 1.2×	12 0.3×	38	425
Christa Dixkens Germany	7	137 0.9×	354 3.5×	15 0.4×	34 1.0×	18 0.5×	9	427

Countries citing papers authored by G.J. te Meerman

Since Specialization

Citations

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

Fields of papers citing papers by G.J. te Meerman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G.J. te Meerman. 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 G.J. te Meerman. The network helps show where G.J. te Meerman may publish in the future.

Co-authorship network of co-authors of G.J. te Meerman

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

All Works

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15 of 15 papers shown

Oostenbrug, Liekele E., Ilja M. Nolte, Elvira Oosterom, et al.. (2006). CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: An association study and pooled analysis. Digestive and Liver Disease. 38(11). 834–845. 24 indexed citations

Trentani, Andrea, et al.. (2003). Immunohistochemical changes induced by repeated footshock stress: revelations of gender-based differences. Neurobiology of Disease. 14(3). 602–618. 32 indexed citations

Nolte, Ilja M. & G.J. te Meerman. (2002). The probability that similar haplotypes are identical by descent. Annals of Human Genetics. 66(3). 195–209. 11 indexed citations

Dørum, Anne, Pål Møller, Erik-Jan Kamsteeg, et al.. (1997). A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing. European Journal of Cancer. 33(14). 2390–2392. 21 indexed citations

Scheffer, Hans, Rein P. Stulp, Edwin Verlind, et al.. (1997). Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosa. Human Genetics. 100(2). 230–235. 14 indexed citations

Meerman, G.J. te, et al.. (1997). Association and haplotype sharing due to identity by descent, with an application to genetic mapping. University of Groningen research database (University of Groningen / Centre for Information Technology). 115–135. 14 indexed citations

Meerman, G.J. te, et al.. (1997). GENETIC MAPPING OF DISEASE GENES. 4 indexed citations

Meerman, G.J. te, Marian van der Meulen, & Lodewijk A. Sandkuijl. (1995). Perspectives of identity by descent (IBD) mapping in founder populations. Clinical & Experimental Allergy. 25(s2). 97–102. 71 indexed citations

Meulen, Marian van der, et al.. (1995). Recurrence risk for germinal mosaics revisited.. Journal of Medical Genetics. 32(2). 102–104. 35 indexed citations

10.

Meerman, G.J. te, Marian van der Meulen, & Lodewijk A. Sandkuijl. (1994). Expected size of shared haplotypes surrounding a common disease gene. The American Journal of Human Genetics. 55. 2 indexed citations

11.

Meerman, G.J. te, et al.. (1993). Linkage analysis by two-dimensional DNA typing.. PubMed. 53(6). 1289–97. 19 indexed citations

12.

Houwen, R. H. J., et al.. (1991). AN OBLIGATE RECOMBINATION BETWEEN THE WILSON DISEASE LOCUS AND THE CLOSE MARKER D13S31. Data Archiving and Networked Services (DANS). 1 indexed citations

13.

Scheffer, Hans, et al.. (1991). LINKAGE ANALYSIS IN FAMILIES WITH PROXIMAL SPINAL MUSCULAR-ATROPHY FROM THE NETHERLANDS. The American Journal of Human Genetics. 49(4). 203–203. 22 indexed citations

14.

Cornel, Martina C., et al.. (1989). OVULATION INDUCTION, INVITRO FERTILIZATION, AND NEURAL-TUBE DEFECTS. The Lancet. 2. 1530–1530. 21 indexed citations

15.

Scheffer, Hans, G.J. te Meerman, Yvonne C. M. Kruize, et al.. (1989). Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.. PubMed. 45(2). 252–60. 35 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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