Aleksandar Rajkovic

9.5k total citations · 1 hit paper
117 papers, 5.6k citations indexed

About

Aleksandar Rajkovic is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Aleksandar Rajkovic has authored 117 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 51 papers in Molecular Biology and 40 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Aleksandar Rajkovic's work include Reproductive Biology and Fertility (36 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers) and Prenatal Screening and Diagnostics (20 papers). Aleksandar Rajkovic is often cited by papers focused on Reproductive Biology and Fertility (36 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers) and Prenatal Screening and Diagnostics (20 papers). Aleksandar Rajkovic collaborates with scholars based in United States, China and Canada. Aleksandar Rajkovic's co-authors include Svetlana A. Yatsenko, Martin M. Matzuk, Youngsok Choi, Urvashi Surti, Patrick M. Catalano, Krishna Jagarlamudi, Alexander N. Yatsenko, Daniel J. Ballow, Megan McGuire and Richard E. Davis and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Aleksandar Rajkovic

116 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

2021 221 citations Anthony R. Gregg, Mahmoud Aarabi et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aleksandar Rajkovic United States	39	2.2k	2.1k	1.8k	1.5k	723	117	5.6k
Darryl L. Russell Australia	47	1.1k 0.5×	2.4k 1.2×	3.9k 2.2×	2.6k 1.8×	951 1.3×	110	7.3k
Geri Méduri France	40	1.1k 0.5×	1.5k 0.7×	1.1k 0.6×	1.7k 1.2×	223 0.3×	93	4.2k
Kunio Shiota Japan	46	1.9k 0.9×	5.3k 2.5×	1.0k 0.6×	497 0.3×	969 1.3×	190	7.3k
Jock K. Findlay Australia	53	1.6k 0.8×	3.9k 1.9×	3.4k 2.0×	3.0k 2.0×	617 0.9×	175	9.2k
Tetsu Yano Japan	47	711 0.3×	1.4k 0.7×	918 0.5×	2.6k 1.8×	510 0.7×	180	6.3k
Philippe Touraine France	44	1.6k 0.7×	2.4k 1.2×	1.5k 0.8×	1.5k 1.0×	516 0.7×	195	6.1k
Hyunjung Jade Lim South Korea	38	1.7k 0.8×	2.4k 1.1×	2.0k 1.2×	2.8k 1.9×	320 0.4×	99	7.5k
M Massobrio Italy	43	799 0.4×	1.5k 0.7×	1.1k 0.6×	1.9k 1.3×	679 0.9×	185	8.1k
Richard L. Cate United States	37	2.3k 1.1×	4.2k 2.0×	2.1k 1.2×	2.2k 1.5×	302 0.4×	65	8.3k
Alan L. Schneyer United States	45	716 0.3×	3.4k 1.6×	1.3k 0.7×	1.2k 0.8×	240 0.3×	112	6.0k

Countries citing papers authored by Aleksandar Rajkovic

Since Specialization

Citations

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

Fields of papers citing papers by Aleksandar Rajkovic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aleksandar Rajkovic

This figure shows the co-authorship network connecting the top 25 collaborators of Aleksandar Rajkovic. A scholar is included among the top collaborators of Aleksandar Rajkovic 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 Aleksandar Rajkovic. Aleksandar Rajkovic 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

Witchel, Selma F., Aleksandar Rajkovic, & Svetlana A. Yatsenko. (2025). Discrepancies Between Sex Prediction and Fetal Sex After Prenatal Noninvasive Cell-Free DNA Screening. Journal of the Endocrine Society. 9(2). bvaf007–bvaf007. 1 indexed citations

Rajkovic, Aleksandar, et al.. (2023). Sohlh1loss of function male and female infertility model impacts overall health beyond gonadal dysfunction in mice. Biology of Reproduction. 108(4). 619–628. 1 indexed citations

Berman, Andrea J., et al.. (2023). Heterozygous TP63 pathogenic variants in isolated primary ovarian insufficiency. Journal of Assisted Reproduction and Genetics. 40(9). 2211–2218. 2 indexed citations

Gregg, Anthony R., Mahmoud Aarabi, Susan Klugman, et al.. (2022). Screening for Autosomal Recessive and X-Linked Conditions During Pregnancy and Preconception: A Practice Resource of the American College of Medical Genetics and Genomics (ACMG). Obstetrical & Gynecological Survey. 77(4). 193–196. 2 indexed citations

Yatsenko, Svetlana A., Mahmoud Aarabi, Jie Hu, et al.. (2020). Copy number alterations involving 59 ACMG ‐recommended secondary findings genes. Clinical Genetics. 98(6). 577–588. 3 indexed citations

Distl, O., Martina Hoedemaker, Rüdiger Behr, et al.. (2020). Loss of Cx43 in Murine Sertoli Cells Leads to Altered Prepubertal Sertoli Cell Maturation and Impairment of the Mitosis-Meiosis Switch. Cells. 9(3). 676–676. 15 indexed citations

Yatsenko, Svetlana A., Michelle A. Wood, Tianjiao Chu, Huaiyang Jiang, & Aleksandar Rajkovic. (2019). A high-resolution X chromosome copy-number variation map in fertile females and women with primary ovarian insufficiency. Genetics in Medicine. 21(10). 2275–2284. 14 indexed citations

Aarabi, Mahmoud, E Kessler, Suneeta Madan‐Khetarpal, et al.. (2018). Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation. European Journal of Medical Genetics. 62(4). 239–242. 12 indexed citations

Gurda, Grzegorz T., Svetlana A. Yatsenko, Aleksandar Rajkovic, et al.. (2017). Synchronous Bilateral Tubal Serous Carcinomas in a Patient With Exon 13 Duplication and Loss of Function of BRCA1. International Journal of Gynecological Pathology. 37(2). 117–122. 2 indexed citations

10.

Dangle, Pankaj, Miguel Reyes‐Múgica, Selma F. Witchel, et al.. (2017). Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region. Journal of Medical Genetics. 54(10). 705–709. 14 indexed citations

11.

Yatsenko, Alexander N., Andrew Georgiadis, Albrecht Röpke, et al.. (2015). X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men. New England Journal of Medicine. 372(22). 2097–2107. 228 indexed citations

12.

Suzuki, Hidenori, et al.. (2013). Spermatogonial SOHLH1 nucleocytoplasmic shuttling associates with initiation of spermatogenesis in the rhesus monkey (Macaca mulatta). Molecular Human Reproduction. 20(4). 350–357. 14 indexed citations

13.

Suzuki, Hitomi, Christina Tenenhaus Dann, & Aleksandar Rajkovic. (2012). Generation of a germ cell‐specific mouse transgenic cherry reporter, Sohlh1‐mCherryFlag. genesis. 51(1). 50–58. 8 indexed citations

14.

Suzuki, Hitomi, Hyo Won Ahn, Tianjiao Chu, et al.. (2011). SOHLH1 and SOHLH2 coordinate spermatogonial differentiation. Developmental Biology. 361(2). 301–312. 151 indexed citations

15.

Choi, Youngsok, Min‐Ho Lee, Miseon Park, et al.. (2010). Mutations in SOHLH1 gene associate with nonobstructive Azoospermia. Human Mutation. 31(7). 788–793. 68 indexed citations

16.

Edlefsen, Kerstin L., Rebecca D. Jackson, Ross L. Prentice, et al.. (2010). The effects of postmenopausal hormone therapy on serum estrogen, progesterone, and sex hormone-binding globulin levels in healthy postmenopausal women. Menopause The Journal of The North American Menopause Society. 17(3). 622–629. 46 indexed citations

17.

Suzumori, Nobuhiro, Stephanie A. Pangas, & Aleksandar Rajkovic. (2007). Candidate Genes for Premature Ovarian Failure. Current Medicinal Chemistry. 14(3). 353–357. 37 indexed citations

18.

Greenbaum, Michael P., Wei Yan, Yi‐Nan Lin, et al.. (2006). TEX14 is essential for intercellular bridges and fertility in male mice. Proceedings of the National Academy of Sciences. 103(13). 4982–4987. 204 indexed citations

19.

Rajkovic, Aleksandar, et al.. (1999). Plasma Homocyst(e)ine Concentrations in Eclamptic and Preeclamptic African Women Postpartum. Obstetrics and Gynecology. 94(3). 355–360. 9 indexed citations

20.

Rajkovic, Aleksandar, et al.. (1997). Elevated homocyst(e)ine levels with preeclampsia. Obstetrics and Gynecology. 90(2). 168–171. 162 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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