World's Best Scientists 2026 revealed!
Evelin Schröck

Evelin Schröck

D-Index & Metrics

Genetics

D-Index
74
Citations
22404
World Ranking
1960
National Ranking
143

Evelin Schröck 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 Evelin Schröck 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: 250 publications — 66th percentile

66% of scientists in this discipline score the same or lower.

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

Evelin Schröck 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 Evelin Schröck 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: 74 D-Index — 56th percentile

56% of scientists in this discipline score the same or lower.

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

Overview

Evelin Schröck is affiliated with TU Dresden in Germany and has contributed extensively to the fields of biochemistry, genetics, molecular biology, and medicine. Their research spans several interconnected subfields including molecular biology, genetics, cancer research, oncology, and pathology and forensic medicine.

Their work covers multiple topics related to cancer and genetics, with notable focus areas such as:

  • Cancer Genomics and Diagnostics
  • Genetic factors in colorectal cancer
  • Genomics and Rare Diseases
  • Epigenetics and DNA Methylation
  • Pancreatic and Hepatic Oncology Research
  • RNA modifications and cancer
  • Genomic variations and chromosomal abnormalities

Schröck has published research in a variety of reputable journals and venues, frequently contributing to:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • European Journal of Human Genetics
  • Cancer Research
  • Nature Communications
  • Medizinische Genetik

Some of the recent papers featuring Schröck's research include:

  • Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers, 2021, Cancer Discovery
  • The landscape of chromothripsis across adult cancer types, 2020, Nature Communications
  • Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome, 2020, European Journal of Human Genetics
  • Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database, 2023, EClinicalMedicine
  • Solving patients with rare diseases through programmatic reanalysis of genome-phenome data, 2021, European Journal of Human Genetics

Collaboration with other researchers forms a significant part of Schröck's work. Frequent co-authors include:

  • Stefan Fröhling
  • Hanno Glimm
  • Christoph Heining
  • Barbara Hutter
  • Peter Horak

Best Publications

  • Multicolor Spectral Karyotyping of Human Chromosomes

    E. Schröck;S. du Manoir;T. Veldman;B. Schoell

  • Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.

    Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland

  • Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3.

    Chesi M;Nardini E;Brents La;Schröck E

  • Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization

    Stanislas du Manoir;Michael R. Speicher;Stefan Joos;Evelin Schröck

  • Role of Chromosome Territories in the Functional Compartmentalization of the Cell Nucleus

    Thomas Cremer;A. Kurz;R. M. Zirbel;S. Dietzel

  • Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix

    K Heselmeyer;E Schröck;S du Manoir;H Blegen

  • Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma

    Marta Chesi;Marta Chesi;P. Leif Bergsagel;P. Leif Bergsagel;Oluwatoyin O. Shonukan;Oluwatoyin O. Shonukan;Maria Luisa Martelli;Maria Luisa Martelli

  • Comparative genomic hybridization reveals a specific pattern of chromosomal gains and losses during the genesis of colorectal tumors.

    Thomas Ried;Regina Knutzen;Rüdiger Steinbeck;Harald Blegen

  • Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping

    Tim Veldman;Christine Vignon;Evelin Schröck;Janet D. Rowley

  • Comprehensive and Definitive Molecular Cytogenetic Characterization of HeLa Cells by Spectral Karyotyping

    M.V.E. Macville;E. Schrock;H.M. Padilla-Nash;C. Keck

  • Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization.

    M R Speicher;B Schoell;S du Manoir;E Schröck

  • Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations†

    B. Michael Ghadimi;Dan L. Sackett;Michael J. Difilippantonio;Evelin Schröck

  • Quantitative analysis of comparative genomic hybridization

    Stanislas du Manoir;Evelin Schröck;Martin Bentz;Michael R. Speicher

  • Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation.

    Thomas Ried;Kerstin Heselmeyer‐Haddad;Kerstin Heselmeyer‐Haddad;Harald Blegen;Evelin Schröck

  • Multicolour spectral karyotyping of mouse chromosomes.

    M Liyanage;A Coleman;S du Manoir;T Veldman

  • Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q

    Kerstin Heselmeyer;Merryn Macville;Evelin Schröck;Harald Blegen

  • Keratin 9 Gene Mutations in Epidermolytic Palmoplantar Keratoderma (EPPK)

    André Reis;Hans Christian Hennies;Lutz Langbein;Martin Digweed

  • Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas

    Ried T;Just Ke;Holtgreve-Grez H;du Manoir S

  • Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization.

    T Ried;I Petersen;H Holtgreve-Grez;M R Speicher

  • Modeling of C/EBPalpha mutant acute myeloid leukemia reveals a common expression signature of committed myeloid leukemia-initiating cells.

    Peggy Kirstetter;Mikkel B Schuster;Oksana Bereshchenko;Susan Moore

Frequent Co-Authors

Thomas Ried
Thomas Ried National Institutes of Health
Barbara Hutter
Barbara Hutter German Cancer Research Center
Hanno Glimm
Hanno Glimm TU Dresden
Benedikt Brors
Benedikt Brors German Cancer Research Center
Albrecht Stenzinger
Albrecht Stenzinger Heidelberg University
Thomas Cremer
Thomas Cremer Ludwig-Maximilians-Universität München
Roland Eils
Roland Eils Charité - University Medicine Berlin
Wilko Weichert
Wilko Weichert Technical University of Munich
Michael R. Speicher
Michael R. Speicher Medical University of Graz
Peter Horak
Peter Horak University of Southampton

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