World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
63
Citations
14648
World Ranking
2888
National Ranking
1262

Aleksandar Rajkovic publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Aleksandar Rajkovic sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 187 publications — 45th percentile

45% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Aleksandar Rajkovic D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Aleksandar Rajkovic sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 63 D-Index — 35th percentile

35% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Aleksandar Rajkovic is affiliated with the University of California, San Francisco in the United States. Their research spans multiple fields, primarily focused on Medicine and Biochemistry, Genetics and Molecular Biology. Within these broader fields, their work covers specific subfields such as Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Obstetrics and Gynecology, and Reproductive Medicine.

The scientist's main topics of investigation include:

  • Prenatal Screening and Diagnostics
  • Genomic variations and chromosomal abnormalities
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Assisted Reproductive Technology and Twin Pregnancy
  • Genomics and Rare Diseases
  • Reproductive System and Pregnancy
  • Genetic factors in colorectal cancer

Rajkovic has published extensively in several academic venues, with frequent contributions to:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics in Medicine
  • American Journal of Medical Genetics Part A
  • Genetics in Medicine Open
  • Human Reproduction

Frequent co-authors in their work include Svetlana A. Yatsenko, Mahmoud Aarabi, Selma F. Witchel, Devereux N. Saller, and Anthony R. Gregg.

Notable recent papers by Aleksandar Rajkovic include:

  • "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, Genetics in Medicine
  • "Testis formation in XX individuals resulting from novel pathogenic variants in Wilms' tumor 1 (WT1) gene", 2020, Proceedings of the National Academy of Sciences
  • "Female reproductive tract has low concentration of SARS-CoV2 receptors", 2020, PLoS ONE
  • "Reproductive outcomes in individuals with chromosomal reciprocal translocations", 2021, Genetics in Medicine
  • "Single-cell sequencing reveals novel cellular heterogeneity in uterine leiomyomas", 2022, Human Reproduction

Best Publications

  • Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

    Laufey Amundadottir;Peter Kraft;Rachael Z. Stolzenberg-Solomon;Charles S. Fuchs

  • A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

    Gloria M. Petersen;Laufey Amundadottir;Charles S. Fuchs;Peter Kraft

  • Breast cancer after use of estrogen plus progestin in postmenopausal women

    Rowan T. Chlebowski;Lewis H. Kuller;Ross L. Prentice;Marcia L. Stefanick

  • NOBOX DEFICIENCY DISRUPTS EARLY FOLLICULOGENESIS AND OOCYTE-SPECIFIC GENE EXPRESSION

    Aleksandar Rajkovic;Stephanie A. Pangas;Daniel Ballow;Nobuhiro Suzumori

  • Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

    Shahana Ahmed;Gilles Thomas;Maya Ghoussaini;Catherine S. Healey

  • X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

    Alexander N. Yatsenko;Andrew P. Georgiadis;Albrecht Röpke;Andrea J. Berman

  • Ovarian differentiation and gonadal failure.

    Joe Leigh Simpson;Aleksandar Rajkovic

  • Oogenesis requires germ cell-specific transcriptional regulators Sohlh1 and Lhx8.

    Stephanie A. Pangas;Youngsok Choi;Daniel J. Ballow;Yangu Zhao

  • TEX14 is essential for intercellular bridges and fertility in male mice

    Michael P. Greenbaum;Wei Yan;Meng-Hsieh Wu;Yi-Nan Lin

  • Pancreatic cancer risk and ABO blood group alleles : results from the pancreatic cancer cohort consortium

    Brian M. Wolpin;Peter Kraft;Myron Gross;Kathy Helzlsouer

  • NOBOX Homeobox Mutation Causes Premature Ovarian Failure

    Yingying Qin;Youngsok Choi;Han Zhao;Han Zhao;Joe Leigh Simpson

  • Sohlh1 is essential for spermatogonial differentiation.

    D. Ballow;M.L. Meistrich;M. Matzuk;A. Rajkovic

  • Correction to: 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).

    Anthony R. Gregg;Mahmoud Aarabi;Mahmoud Aarabi;Susan Klugman;Natalia T. Leach

  • Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis.

    Yong Hyun Shin;Youngsok Choi;Serpil Uckac Erdin;Svetlana A. Yatsenko

  • Transcription Factor FIGLA is Mutated in Patients with Premature Ovarian Failure

    Han Zhao;Zi-Jiang Chen;Yingying Qin;Yuhua Shi

  • Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.

    Saleh AlAsiri;Sulman Basit;Michelle A. Wood-Trageser;Svetlana A. Yatsenko

  • Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome

    David Peters;Tianjiao Chu;Svetlana A. Yatsenko;Nancy Hendrix

  • MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability

    Michelle A. Wood-Trageser;Fatih Gurbuz;Svetlana A. Yatsenko;Elizabeth P. Jeffries

  • Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes

    Nobuhiro Suzumori;Changning Yan;Martin M. Matzuk;Aleksandar Rajkovic

  • Genetics of human female infertility

    Svetlana A Yatsenko;Aleksandar Rajkovic

Frequent Co-Authors

Urvashi Surti
Urvashi Surti University of Pittsburgh
Dimitrios Trichopoulos
Dimitrios Trichopoulos Harvard University
Martin M. Matzuk
Martin M. Matzuk Baylor College of Medicine
Kevin B. Jacobs
Kevin B. Jacobs Progenity (United States)
J. Michael Gaziano
J. Michael Gaziano Brigham and Women's Hospital
Stephen J. Chanock
Stephen J. Chanock National Institutes of Health
Dominique S. Michaud
Dominique S. Michaud Tufts University
Wei Zheng
Wei Zheng Vanderbilt University Medical Center
Charles Kooperberg
Charles Kooperberg Fred Hutchinson Cancer Research Center
Susan E. Hankinson
Susan E. Hankinson University of Massachusetts Amherst

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