T. Mohandas

1.4k total citations
39 papers, 1.1k citations indexed

About

T. Mohandas is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, T. Mohandas has authored 39 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T. Mohandas's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (12 papers) and Genetic Syndromes and Imprinting (6 papers). T. Mohandas is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (12 papers) and Genetic Syndromes and Imprinting (6 papers). T. Mohandas collaborates with scholars based in United States, Japan and Italy. T. Mohandas's co-authors include Jonathan P. Park, Merry Passage, P. H. Seeburg, C.-M. Becker, Larry J. Shapiro, Peter R. Schofield, Gabriele Grenningloh, Volker Schmieden, Teepu Siddique and Heinrich Betz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The EMBO Journal.

In The Last Decade

T. Mohandas

36 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Mohandas United States 18 627 463 260 202 111 39 1.1k
Nadine Gigarel France 18 1.8k 2.9× 282 0.6× 248 1.0× 194 1.0× 78 0.7× 39 2.2k
Sharon Zeligson Israel 19 731 1.2× 281 0.6× 166 0.6× 167 0.8× 51 0.5× 41 1.3k
Carol Saunders United States 22 744 1.2× 635 1.4× 110 0.4× 93 0.5× 72 0.6× 59 1.3k
Alexandra Afenjar France 16 521 0.8× 621 1.3× 113 0.4× 106 0.5× 50 0.5× 42 1.0k
Ivo Kremensky Bulgaria 18 753 1.2× 295 0.6× 84 0.3× 395 2.0× 104 0.9× 75 1.4k
Reeval Segel Israel 18 649 1.0× 249 0.5× 211 0.8× 69 0.3× 87 0.8× 40 1.1k
Monika Cohen Germany 11 551 0.9× 488 1.1× 98 0.4× 113 0.6× 49 0.4× 13 859
Séverine Drunat France 21 581 0.9× 443 1.0× 144 0.6× 36 0.2× 150 1.4× 57 1.1k
Thomas F. Wienker Germany 20 658 1.0× 382 0.8× 40 0.2× 171 0.8× 51 0.5× 59 1.3k
Olga A. Cabello United States 9 1.0k 1.6× 583 1.3× 90 0.3× 130 0.6× 52 0.5× 10 1.2k

Countries citing papers authored by T. Mohandas

Since Specialization
Citations

This map shows the geographic impact of T. Mohandas'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 T. Mohandas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Mohandas more than expected).

Fields of papers citing papers by T. Mohandas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Mohandas

This figure shows the co-authorship network connecting the top 25 collaborators of T. Mohandas. A scholar is included among the top collaborators of T. Mohandas 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 T. Mohandas. T. Mohandas 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.
Park, Jonathan P., et al.. (2001). Prenatal diagnosis of mosaic tetrasomy 5p. Prenatal Diagnosis. 21(5). 351–353. 6 indexed citations
2.
Park, Jonathan P., et al.. (2000). Amplification of the MLL Region in Acute Myeloid Leukemia. Cancer Genetics and Cytogenetics. 121(2). 198–205. 17 indexed citations
3.
Mohandas, T., Richard A. Spellman, James J. Filiano, et al.. (1999). Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay. American Journal of Medical Genetics. 82(4). 294–300. 64 indexed citations
4.
Park, Jonathan P., et al.. (1998). Smith‐Magenis syndrome resulting from a de novo direct insertion of proximal 17q into 17p11.2. American Journal of Medical Genetics. 77(1). 23–27. 1 indexed citations
5.
Spellman, Richard A., et al.. (1998). Human chromosome 9 pericentric homologies: implications for chromosome 9 heteromorphisms. Cytogenetic and Genome Research. 82(3-4). 192–194. 24 indexed citations
6.
Park, Jonathan P., et al.. (1997). Diffuse Large Cell, B-cell Type Lymphoma with a Novel Translocation (2;22)(p23;q11.2). Cancer Genetics and Cytogenetics. 96(2). 118–122. 18 indexed citations
7.
Nishita, Yoshinori, et al.. (1997). Reactivation of an Inactive Human X Chromosome Introduced into Mouse Embryonal Carcinoma Cells by Microcell Fusion with Persistent Expression ofXIST. Experimental Cell Research. 230(2). 208–219. 17 indexed citations
8.
Mohandas, T., Lucy B. Rowe, E H Birkenmeier, et al.. (1995). Localization of the Tight Junction Protein Gene TJP1 to Human Chromosome 15q13, Distal to the Prader-Willi/Angelman Region, and to Mouse Chromosome 7. Genomics. 30(3). 594–597. 9 indexed citations
9.
Wells, Rebecca G., T. Mohandas, & Matthias A. Hediger. (1993). Localization of the Na+/Glucose Cotransporter Gene SGLT2 to Human Chromosome 16 Close to the Centromere. Genomics. 17(3). 787–789. 50 indexed citations
10.
Ellison, Jay W., et al.. (1992). Directed isolation of human genes that escape X inactivation. Somatic Cell and Molecular Genetics. 18(3). 259–268. 30 indexed citations
11.
Williams, John, et al.. (1992). Apparent non‐mosaic trisomy 16 in chorionic villi: Diagnostic dilemma or clinically significant finding?. Prenatal Diagnosis. 12(3). 163–168. 27 indexed citations
12.
Grenningloh, Gabriele, Volker Schmieden, Peter R. Schofield, et al.. (1990). Alpha subunit variants of the human glycine receptor: primary structures, functional expression and chromosomal localization of the corresponding genes.. The EMBO Journal. 9(3). 771–776. 243 indexed citations
13.
Azuma, Takeshi, et al.. (1990). Assignment of cathepsin E (CTSE) to human chromosome region 1q31 by in situ hybridization and analysis of somatic cell hybrids. Cytogenetic and Genome Research. 53(2-3). 137–139. 8 indexed citations
14.
Shohat, Mordechai, Tami Shohat, D L Rimoin, et al.. (1990). Rearrangement of chromosome 15 in the region q11.2→q12 in an individual with obesity syndrome and her normal mother. American Journal of Medical Genetics. 37(2). 173–177. 11 indexed citations
15.
Yoshida, Akira, Lily C. Hsu, Tohru Ikuta, et al.. (1988). Molecular genetics of alcohol-metabolizing enzymes. Biochemical Society Transactions. 16(3). 230–232. 4 indexed citations
16.
Mohandas, T., et al.. (1985). Marker Chromosomes: Cytogenetic characterization and implications for prenatal diagnosis. American Journal of Medical Genetics. 20(2). 361–368. 15 indexed citations
17.
Blumberg, Bruce, et al.. (1982). Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.. PubMed. 34(6). 948–60. 26 indexed citations
18.
Frydman, Moshe, David A. Greenberg, T. Mohandas, & Michael M. Kaback. (1982). Comparison of fetal and maternal chromosome polymorphisms: Applications in prenatal diagnosis. Prenatal Diagnosis. 2(1). 25–31. 8 indexed citations
19.
Sparkes, Robert S., et al.. (1978). Aconitase (E.C. 4.2.1.3) mitochondrial locus mapped to human chromosome 22: Studies with Chinese hamster-human somatic cell hybrids. Biochemical Genetics. 16(7-8). 751–756. 5 indexed citations
20.
Barker, P E, T. Mohandas, & Michael M. Kaback. (1977). Chromosome polymorphisms in karyotypes from amniotic fluid cell cultures. Clinical Genetics. 11(3). 243–248. 27 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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