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Genetics
Austria
2025

D-Index & Metrics

Genetics

D-Index
73
Citations
55984
World Ranking
1993
National Ranking
9

Research.com Recognitions

  • 2025 - Research.com Genetics in Austria Leader Award

Overview

André Rosenthal is affiliated with the Institute of Molecular Biotechnology in Austria. Their research spans multiple areas predominantly in medicine and engineering, with six publications in each field. The scientist's work covers various subfields including nuclear and high energy physics, public health, environmental and occupational health, pediatrics, perinatology and child health, molecular biology, and aerospace engineering.

Rosenthal has contributed to research on topics such as magnetic confinement fusion research, reproductive biology and fertility, ovarian function and disorders, assisted reproductive technology and twin pregnancy, fusion materials and technologies, superconducting materials and applications, and renal and related cancers.

Frequent collaborators in Rosenthal's publications include Johan Smitz, Inge Van Vaerenbergh, Tom Adriaenssens, Wim Coucke, and L. Van Landuyt.

Some of the recent papers authored or co-authored by André Rosenthal are:

  • Improved clinical outcomes after non-invasive oocyte selection and Day 3 eSET in ICSI patients, 2021, Reproductive Biology and Endocrinology
  • Enhanced pedestal transport driven by edge collisionality on Alcator C-Mod and its role in regulating H-mode pedestal gradients, 2024, Nuclear Fusion
  • Non-invasive cumulus cell analysis can be applied for oocyte ranking and is useful for countries with legal restrictions on embryo generation or freezing, 2024, PLoS ONE
  • A 1D Lyman-alpha Profile Camera for Plasma Edge Neutral Studies on the DIII-D Tokamak, 2021, OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)
  • Enhanced pedestal transport driven by edge collisionality on Alcator C-Mod and its role in regulating H-mode pedestal gradients, 2024, arXiv (Cornell University)

Rosenthal frequently publishes in the following venues:

  • Reproductive Biology and Endocrinology
  • arXiv (Cornell University)
  • Nuclear Fusion
  • PLoS ONE
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)

Best Publications

  • Initial sequencing and analysis of the human genome.

    Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum

  • The genome of the social amoeba Dictyostelium discoideum

    L. Eichinger;J. A. Pachebat;J. A. Pachebat;G. Glöckner;M.-A. Rajandream

  • The DNA sequence of human chromosome 21

    M. Hattori;A. Fujiyama;T. D. Taylor;H. Watanabe

  • The DNA sequence of the human X chromosome

    Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer

  • Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

    Raymonda Varon;Christine Vissinga;Matthias Platzer;Karen M Cerosaletti

  • Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

    Ercole Rao;Birgit Weiss;Maki Fukami;Maki Fukami;Andreas Rump

  • Bisulfite genomic sequencing: systematic investigation of critical experimental parameters

    Christoph Grunau;S. J. Clark;André Rosenthal

  • Molecular basis of symbiosis between Rhizobium and legumes

    Christoph Freiberg;Remy Fellay;Amos Marc Bairoch;William John Broughton

  • A physical map of the human genome.

    John Douglas Mcpherson;Marco Marra;Marco Marra;La Deana Hillier;Robert H. Waterston

  • An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

    Tim M. Strom;Gerald Nyakatura;Eckart Apfelstedt-Sylla;Heide Hellebrand

  • X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.

    Monique Jouet;André Rosenthal;Giles Armstrong;John MacFarlane

  • N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.

    Luba Kalaydjieva;Luba Kalaydjieva;David Gresham;Rebecca Gooding;Lisa Heather

  • Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32).

    Quangeng Zhang;Reiner Siebert;Minhong Yan;Bernd Hinzmann

  • Positional cloning of the gene for X-linked retinitis pigmentosa 2

    U. Schwahn;S. Lenzner;J Dong;S. Feil

  • WIF1, a component of the Wnt pathway, is down-regulated in prostate, breast, lung, and bladder cancer.

    Christoph Wissmann;Peter Johannes Wild;Simone Kaiser;Stefan Roepcke

  • Discovery of new human β-defensins using a genomics-based approach

    Hong Peng Jia;Brian C. Schutte;Andreas Schudy;Rose Linzmeier

  • Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X–linked hydrocephalus

    André Rosenthal;Monique Jouet;Susan Kenwrick

  • Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

    Philomena Mburu;Mirna Mustapha;Anabel Varela;Dominique Weil

  • Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.

    P. Momeni;G. Glöckner;O. Schmidt;D. Von Holtum

  • N-MYC Downstream-Regulated Gene 1 Is Mutated In Hereditary Motor And Sensory Neuropathy-LOM

    L Kalaydjieva;D Gresham;R Gooding;L Heather

Frequent Co-Authors

Edgar Dahl
Edgar Dahl RWTH Aachen University
Matthias Platzer
Matthias Platzer Leibniz Association
Stefan Taudien
Stefan Taudien Universitätsmedizin Göttingen
Hans Lehrach
Hans Lehrach Max Planck Society
Christine Sers
Christine Sers Charité - University Medicine Berlin
Masahira Hattori
Masahira Hattori Waseda University
Gernot Glöckner
Gernot Glöckner University of Cologne
Nobuyoshi Shimizu
Nobuyoshi Shimizu Keio University
Sydney Brenner
Sydney Brenner Agency for Science, Technology and Research

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