M. Verjaal

711 total citations
25 papers, 457 citations indexed

About

M. Verjaal is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, M. Verjaal has authored 25 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pediatrics, Perinatology and Child Health, 12 papers in Genetics and 6 papers in Surgery. Recurrent topics in M. Verjaal's work include Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic Syndromes and Imprinting (5 papers). M. Verjaal is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic Syndromes and Imprinting (5 papers). M. Verjaal collaborates with scholars based in Netherlands, United Kingdom and France. M. Verjaal's co-authors include N. J. Leschot, P.E. Treffers, Hans Wolf, Pieter E. Treffers, G. C. M. L. Christiaens, H. H. H. Kanhai, Humphrey H.H. Kanhai, K. Madan, P. Pearson and Juul Wijnen and has published in prestigious journals such as BJOG An International Journal of Obstetrics & Gynaecology, Journal of Medical Genetics and Human Genetics.

In The Last Decade

M. Verjaal

24 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Verjaal Netherlands 12 293 237 101 83 44 25 457
Kamal K. Naguib Kuwait 14 140 0.5× 269 1.1× 189 1.9× 95 1.1× 72 1.6× 40 558
R. Rauskolb Germany 14 196 0.7× 128 0.5× 82 0.8× 99 1.2× 11 0.3× 41 379
Mary Lucas United Kingdom 14 186 0.6× 239 1.0× 152 1.5× 38 0.5× 14 0.3× 24 475
MarkW. Steele United States 5 234 0.8× 122 0.5× 59 0.6× 117 1.4× 26 0.6× 7 361
Maria Mercedes de Elejalde United States 11 162 0.6× 174 0.7× 70 0.7× 96 1.2× 17 0.4× 21 342
Cantú Jm Mexico 12 104 0.4× 259 1.1× 165 1.6× 41 0.5× 40 0.9× 67 405
Pamela Renwick United Kingdom 9 237 0.8× 124 0.5× 121 1.2× 47 0.6× 52 1.2× 10 363
Andrea Nuccitelli Italy 10 446 1.5× 256 1.1× 104 1.0× 75 0.9× 37 0.8× 16 593
Glenn Atkinson United Kingdom 8 334 1.1× 153 0.6× 87 0.9× 76 0.9× 24 0.5× 9 497
A. Caine United Kingdom 7 118 0.4× 252 1.1× 124 1.2× 27 0.3× 10 0.2× 9 363

Countries citing papers authored by M. Verjaal

Since Specialization
Citations

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

Fields of papers citing papers by M. Verjaal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Verjaal

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

All Works

20 of 20 papers shown
1.
Berg, Henk van den, et al.. (2000). Prenatal HLA-matching to determine suitability for allogeneic bone marrow transplantation. Bone Marrow Transplantation. 25(6). 579–581. 7 indexed citations
2.
Leschot, N. J., M. Verjaal, Kerstin Hansson, et al.. (1996). THE OUTCOME OF PREGNANCIES WITH CONFINED PLACENTAL CHROMOSOME MOSAICISM IN CYTOTROPHOBLAST CELLS. Prenatal Diagnosis. 16(8). 705–712. 25 indexed citations
3.
Leschot, N. J., H. H. H. Kanhai, C. J. van Asperen, et al.. (1990). An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS. Clinical Genetics. 38(3). 211–217. 9 indexed citations
4.
Leschot, N. J., et al.. (1990). Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma. Clinical Genetics. 37(3). 236–237. 4 indexed citations
5.
Leschot, N. J., Hans Wolf, C. J. van Asperen, et al.. (1989). Cytogenetic findings in 1250 chorionic villus samples obtained in the first trimester with clinical follow‐up of the first 1000 pregnancies. BJOG An International Journal of Obstetrics & Gynaecology. 96(6). 663–670. 33 indexed citations
6.
Leschot, N. J., et al.. (1988). Chorionic Villi Sampling. Obstetrical & Gynecological Survey. 43(3). 155–156. 1 indexed citations
7.
Breuning, M.H., K. Madan, M. Verjaal, et al.. (1987). Human ?-globin maps to pter-p13.3 in chromosome 16 distal to PGP. Human Genetics. 76(3). 287–9. 34 indexed citations
8.
Visser, M., B.W. Ongerboer de Visser, & M. Verjaal. (1987). A family with pyramidal features and amyotrophy of the hands. Clinical Neurology and Neurosurgery. 89(2). 125–125.
9.
Verjaal, M., et al.. (1987). Karyotypic differences between cells from placenta and other fetal tissues. Prenatal Diagnosis. 7(5). 343–348. 23 indexed citations
10.
Leschot, N. J., M. Verjaal, & Pieter E. Treffers. (1985). A critical analysis of 75 therapeutic abortions. Early Human Development. 10(3-4). 287–293. 6 indexed citations
11.
Verjaal, M., N. J. Leschot, & Pieter E. Treffers. (1982). Women's experiences with second trimester prenatal diagnosis. Prenatal Diagnosis. 2(3). 195–209. 27 indexed citations
12.
Verjaal, M., N. J. Leschot, & Pieter E. Treffers. (1981). Risk of amniocentesis and laboratory findings in a series of 1500 prenatal diagnoses. Prenatal Diagnosis. 1(3). 173–181. 27 indexed citations
13.
Leschot, N. J., et al.. (1980). Severe congenital skin defects in a newborn. European Journal of Obstetrics & Gynecology and Reproductive Biology. 10(6). 381–388. 28 indexed citations
14.
Treffers, P.E., et al.. (1979). Prenatal diagnosis of congenital malformations in 500 pregnancies. European Journal of Obstetrics & Gynecology and Reproductive Biology. 9(1). 13–22. 9 indexed citations
15.
Leschot, N. J., et al.. (1979). Five familial cases with a trisomy 16p syndrome due to translocation. Clinical Genetics. 16(3). 205–214. 26 indexed citations
16.
Leschot, N. J., et al.. (1978). Prenatal diagnosis of Meckel syndrome. Human Genetics. 43(3). 333–336. 14 indexed citations
17.
Verjaal, M., et al.. (1978). Bilateral renal agenesis (Potter's syndrome) in two consecutive infants. European Journal of Obstetrics & Gynecology and Reproductive Biology. 8(3). 137–142. 3 indexed citations
18.
Verjaal, M., et al.. (1978). Prenatal diagnosis of a de novo Y/22 translocation.. Journal of Medical Genetics. 15(6). 475–479. 9 indexed citations
19.
Verjaal, M.. (1978). A Patient With a Partial Deletion of the Short Arm of Chromosome 3. American journal of diseases of children. 132(1). 43–43. 60 indexed citations
20.
Hösli, P., et al.. (1977). Rapid prenatal diagnosis of HG-PRT deficiency using ultra-microchemical methods. Human Genetics. 37(2). 195–200. 6 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kamal K. Naguib Breakdown of academic impact, for papers by R. Rauskolb Breakdown of academic impact, for papers by Mary Lucas Breakdown of academic impact, for papers by MarkW. Steele Breakdown of academic impact, for papers by Maria Mercedes de Elejalde Breakdown of academic impact, for papers by Cantú Jm Breakdown of academic impact, for papers by Pamela Renwick Breakdown of academic impact, for papers by Andrea Nuccitelli Breakdown of academic impact, for papers by Glenn Atkinson Breakdown of academic impact, for papers by A. Caine
Rankless by CCL
2026