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

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

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

If you’re considering a career in genetics, you may also be interested in related degree options and flexible education models. Many students explore online schools for medical billing and coding as an alternative pathway in the healthcare sector. These programs can provide foundational knowledge of healthcare systems useful for genetics careers.

For those looking to accelerate their education, fast track degree programs offer the chance to complete your studies in less time. This can be ideal if you want to join the workforce sooner or start your postgraduate studies earlier.

Flexibility is key for many learners. A self paced online degree allows you to balance your studies with work, family, or other commitments. This can be especially beneficial if you are managing multiple responsibilities while pursuing your interests in genetics or allied fields.

If you’re concerned about upfront costs, consider applying to no application fee universities. This helps you keep your options open without financial barriers at the application stage.

Best Scientists Citing Evelin Schröck

Trending Scientists