K. Madan

2.8k total citations
50 papers, 1.9k citations indexed

About

K. Madan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, K. Madan has authored 50 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 23 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in K. Madan's work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (19 papers) and Chromosomal and Genetic Variations (18 papers). K. Madan is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (19 papers) and Chromosomal and Genetic Variations (18 papers). K. Madan collaborates with scholars based in Netherlands, United Kingdom and Poland. K. Madan's co-authors include Martin Bobrow, P. Pearson, Aggie Nieuwint, Yolande van Bever, F. H. Menko, Martijn H. Breuning, J. Schoemaker, Kerstin Hansson, S. Walker and C. E. Ford and has published in prestigious journals such as The Lancet, The Journal of Pediatrics and Human Reproduction.

In The Last Decade

K. Madan

50 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Madan Netherlands	26	1.2k	759	693	613	148	50	1.9k
Gesa Schwanitz Germany	22	1.1k 0.9×	532 0.7×	418 0.6×	696 1.1×	140 0.9×	132	1.6k
Dorothy Warburton United States	23	920 0.8×	549 0.7×	331 0.5×	499 0.8×	100 0.7×	35	1.5k
John R. Gosden United Kingdom	27	1.1k 0.9×	1.4k 1.9×	1.1k 1.5×	307 0.5×	101 0.7×	69	2.3k
Heike Starke Germany	25	1.7k 1.4×	967 1.3×	1.2k 1.7×	686 1.1×	61 0.4×	70	2.2k
Philippos C. Patsalis Cyprus	27	1.2k 1.0×	1.0k 1.4×	266 0.4×	705 1.2×	137 0.9×	100	2.0k
W. Roy Breg United States	29	1.6k 1.3×	898 1.2×	538 0.8×	892 1.5×	107 0.7×	73	2.5k
Heinz-Ulrich Weier United States	13	658 0.5×	1.1k 1.5×	363 0.5×	270 0.4×	132 0.9×	16	1.8k
E. Boyd United Kingdom	22	804 0.7×	623 0.8×	304 0.4×	233 0.4×	117 0.8×	55	1.3k
Ram S. Verma United States	23	1.5k 1.2×	1.3k 1.7×	1.2k 1.8×	485 0.8×	50 0.3×	211	2.8k
Avirachan T. Tharapel United States	19	976 0.8×	443 0.6×	274 0.4×	881 1.4×	41 0.3×	61	1.5k

Countries citing papers authored by K. Madan

Since Specialization

Citations

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

Fields of papers citing papers by K. Madan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Madan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Madan, K.. (2020). Natural human chimeras: A review. European Journal of Medical Genetics. 63(9). 103971–103971. 37 indexed citations

Madan, K. & Martijn H. Breuning. (2013). Impact of prenatal technologies on the sex ratio in India: an overview. Genetics in Medicine. 16(6). 425–432. 35 indexed citations

Madan, K., et al.. (2012). An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophy. European Journal of Human Genetics. 21(1). 21–26. 45 indexed citations

Madan, K.. (2012). Balanced complex chromosome rearrangements: Reproductive aspects. A review. American Journal of Medical Genetics Part A. 158A(4). 947–963. 77 indexed citations

Hes, Frederik J., K. Madan, Károly Szuhai, et al.. (2009). Multiple genomic aberrations in a patient with mental retardation and hypogonadism: 45,X/46,X,psu dic(Y) karyotype, thyroid hormone receptor beta (THRB) mutation and heterozygosity for Wilson disease. American Journal of Medical Genetics Part A. 149A(10). 2231–2235. 2 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

Terhal, Pauline, Ralph J. B. Sakkers, Ron Hochstenbach, et al.. (2004). Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism. American Journal of Medical Genetics Part A. 130A(4). 410–414. 13 indexed citations

Ruijs, Mariëlle, et al.. (2002). Atypical progeroid syndrome: An unknown helicase gene defect?. American Journal of Medical Genetics Part A. 116A(3). 295–299. 32 indexed citations

Hamers, A.J.H., Roel Hordijk, Kerstin Hansson, et al.. (1998). Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. European Journal of Human Genetics. 6(3). 194–200. 82 indexed citations

10.

Kwee, M. L., Jerome R. Lo Ten Foe, F. Arwert, et al.. (1996). EARLY PRENATAL DIAGNOSIS OF FANCONI ANAEMIA IN A TWIN PREGNANCY, USING DNA ANALYSIS. Prenatal Diagnosis. 16(4). 345–348. 7 indexed citations

11.

Madan, K.. (1995). Paracentric inversions: a review. Human Genetics. 96(5). 503–15. 81 indexed citations

12.

Madan, K. & F. H. Menko. (1992). Intrachromosomal insertions: a case report and a review. Human Genetics. 89(1). 1–9. 62 indexed citations

13.

Menko, F. H., et al.. (1992). Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33‐qter. American Journal of Medical Genetics. 44(5). 696–698. 18 indexed citations

14.

Madan, K., M.H.E.C. Pieters, L. P. Kuyt, et al.. (1990). Paracentric inversion inv(11) (q21q23) in the Netherlands. Human Genetics. 85(1). 15–20. 11 indexed citations

15.

Madan, K., et al.. (1987). Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly. Human Genetics. 77(2). 193–196. 29 indexed citations

16.

Madan, K., M. Seabright, R H Lindenbaum, & Martin Bobrow. (1984). Paracentric inversions in man.. Journal of Medical Genetics. 21(6). 407–412. 39 indexed citations

17.

Bijvoet, O. L. M., P. Meera Khan, Erna van Loghem, et al.. (1984). Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): Linkage studies in a large Dutch family. Human Genetics. 67(4). 452–454. 4 indexed citations

18.

Madan, K., C. E. Ford, & Cécile Polge. (1978). A reciprocal translocation, t(6p+; 14q−), in the pig. Reproduction. 53(2). 395–398. 18 indexed citations

19.

Madan, K. & Martin Bobrow. (1974). Structural variation in chromosome No 9.. PubMed. 17(2). 81–6. 62 indexed citations

20.

Taysi, Kutay, et al.. (1973). Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome. The Journal of Pediatrics. 82(2). 263–268. 34 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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