N. J. Leschot

3.4k total citations
94 papers, 2.3k citations indexed

About

N. J. Leschot is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, N. J. Leschot has authored 94 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Pediatrics, Perinatology and Child Health, 42 papers in Genetics and 20 papers in Molecular Biology. Recurrent topics in N. J. Leschot's work include Prenatal Screening and Diagnostics (61 papers), Genomic variations and chromosomal abnormalities (23 papers) and Congenital Anomalies and Fetal Surgery (14 papers). N. J. Leschot is often cited by papers focused on Prenatal Screening and Diagnostics (61 papers), Genomic variations and chromosomal abnormalities (23 papers) and Congenital Anomalies and Fetal Surgery (14 papers). N. J. Leschot collaborates with scholars based in Netherlands, United Kingdom and France. N. J. Leschot's co-authors include Mariëtte Goddijn, Fulco van der Veen, M. Verjaal, Johanna C. Korevaar, J.M.N. Hoovers, Hans Wolf, Sjoerd Repping, Patrick M. Bossuyt, P.E. Treffers and Pieter E. Treffers and has published in prestigious journals such as Neurology, Human Reproduction and Fertility and Sterility.

In The Last Decade

N. J. Leschot

92 papers receiving 2.2k citations

Peers

N. J. Leschot

PPCH

GENET

PHEOH

IMMUN

Deborah E. McFadden Canada

G. Harton United States

Joanne Traeger‐Synodinos Greece

Kiyonori Miura Japan

Laird G. Jackson United States

Céline Moutou France

Faustina Lalatta Italy

W. Allen Hogge United States

Yuval Yaron Israel

Giuseppe Simoni Italy

Deborah E. McFadden Canada

N. J. Leschot

1.7k ×1.4

PPCH

1.0k ×1.1

GENET

1.4k ×2.1

724 ×1.7

PHEOH

192 ×0.7

IMMUN

Citations per year, relative to N. J. Leschot N. J. Leschot (= 1×) peers Deborah E. McFadden

Countries citing papers authored by N. J. Leschot

Since Specialization

Citations

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

Fields of papers citing papers by N. J. Leschot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. J. Leschot. 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 N. J. Leschot. The network helps show where N. J. Leschot may publish in the future.

Co-authorship network of co-authors of N. J. Leschot

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

All Works

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20 of 20 papers shown

Boogaard, E. van den, Rosella Hermens, N. J. Leschot, et al.. (2010). Identification of barriers for good adherence to a guideline on recurrent miscarriage. Acta Obstetricia Et Gynecologica Scandinavica. 90(2). 186–191. 12 indexed citations

Twisk, Moniek, N. J. Leschot, Cor Oosterwijk, et al.. (2009). Perspectives of couples with high risk of transmitting genetic disorders. Fertility and Sterility. 94(4). 1239–1243. 25 indexed citations

Vansenne, Fleur, Corianne A.J.M. de Borgie, Johanna C. Korevaar, et al.. (2009). Low uptake of prenatal diagnosis after established carrier status of a balanced structural chromosome abnormality in couples with recurrent miscarriage. Fertility and Sterility. 94(1). 296–300.e3. 2 indexed citations

Aalfs, Cora M., Ellen M.A. Smets, & N. J. Leschot. (2007). Genetic Counselling for Familial Conditions during Pregnancy: A Review of the Literature Published during the Years 1989–2004. Public Health Genomics. 10(3). 159–168. 2 indexed citations

Franssen, Maureen T.M., et al.. (2007). Management of recurrent miscarriage: evaluating the impact of a guideline. Human Reproduction. 22(5). 1298–1303. 23 indexed citations

Westerveld, G.H., Cindy M. Korver, Ans M. M. van Pelt, et al.. (2006). Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure. Human Reproduction. 21(12). 3178–3184. 48 indexed citations

Franssen, Maureen T.M., Johanna C. Korevaar, Fulco van der Veen, et al.. (2006). Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control study. BMJ. 332(7544). 759–763. 100 indexed citations

Franssen, Maureen, Johanna C. Korevaar, N. J. Leschot, et al.. (2005). Selective chromosome analysis in couples with two or more miscarriages: case-control study. BMJ. 331(7509). 137–141. 94 indexed citations

Westerveld, G.H., Sjoerd Repping, N. J. Leschot, Fulco van der Veen, & Maria Lombardi. (2005). Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis. Fertility and Sterility. 83(2). 513–515. 12 indexed citations

10.

Bergen, Arthur A., et al.. (2004). [From gene to disease; primary open-angle glaucoma and three known genes: MYOC, CYP1B1 and OPTN].. PubMed. 148(27). 1343–4. 4 indexed citations

11.

Vries, Jan W. A. de, Mariëtte J.V. Hoffer, Sjoerd Repping, et al.. (2002). Reduced copy number of DAZ genes in subfertile and infertile men. Fertility and Sterility. 77(1). 68–75. 45 indexed citations

12.

Vries, Jan W. A. de, Sjoerd Repping, Saskia K.M. van Daalen, et al.. (2002). Clinical relevance of partial AZFc deletions. Fertility and Sterility. 78(6). 1209–1214. 17 indexed citations

13.

Goddijn, Mariëtte & N. J. Leschot. (2000). Genetic aspects of miscarriage. Best Practice & Research Clinical Obstetrics & Gynaecology. 14(5). 855–865. 172 indexed citations

14.

Leschot, N. J., et al.. (1997). Prenatal Diagnosis in the Netherlands. European Journal of Human Genetics. 5(1). 51–56. 2 indexed citations

15.

Leschot, N. J. & Lars O. Vejerslev. (1997). Proceedings of the EUCROMIC Workshop on Prenatal Diagnosis. European Journal of Human Genetics. 5(1). 1–6. 11 indexed citations

16.

Bleiker, Eveline M. A., Neil K. Aaronson, Fred H. Menko, et al.. (1997). Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members. Patient Education and Counseling. 32(1-2). 107–116. 60 indexed citations

17.

Mannens, M., J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, et al.. (1991). The distal region of 11p13 and associated genetic diseases. Genomics. 11(2). 284–293. 19 indexed citations

18.

Christiaens, G. C. M. L., Joop van Baarlen, Jason S. Huber, & N. J. Leschot. (1989). Fetal limb constriction: A possible complication of CVS. Prenatal Diagnosis. 9(1). 67–71. 24 indexed citations

19.

Ronde, Anthony de, Marcel M. A. M. Mannens, Rosalyn Slater, et al.. (1988). Morphological Transformation by Early Region Human Polyomavirus BK DNA of Human Fibroblasts with Deletions in the Short Arm of One Chromosome 11. Journal of General Virology. 69(2). 467–471. 9 indexed citations

20.

Bröcker-Vriends, A, E Briët, H. H. H. Kanhai, et al.. (1988). First trimester prenatal diagnosis of haemophilia A: Two years' experience. Prenatal Diagnosis. 8(6). 411–421. 8 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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