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Genetics
Germany
2024
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Genetics and Molecular Biology
Germany
2024

D-Index & Metrics

Genetics

D-Index
105
Citations
42752
World Ranking
626
National Ranking
50

Medicine

D-Index
106
Citations
43496
World Ranking
6507
National Ranking
371

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award

Overview

André Reis is affiliated with the University of Erlangen-Nuremberg in Germany. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with extensive work also intersecting Medicine. The scientist's contributions encompass various subfields including Molecular Biology, Genetics, Nephrology, Oncology, and Immunology.

The scientist's work focuses on several main topics, notably Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic Variations and Chromosomal Abnormalities, Congenital Heart Defects Research, Chronic Kidney Disease and Diabetes, RNA Research and Splicing, and Cancer-related Gene Regulation.

André Reis has published in various high-profile venues with notable frequency. The most common publication platforms include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics in Medicine
  • Clinical Genetics
  • European Journal of Human Genetics
  • European Journal of Medical Genetics

Several recent papers illustrate the scope of their research contributions:

  • "Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases" (2020) in The American Journal of Human Genetics
  • "Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease" (2021) in Journal of the American College of Cardiology
  • "Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior" (2021) in Genetics in Medicine
  • "Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis" (2020) in Journal of Investigative Dermatology
  • "Mutations in BRCA1/2 and Other Panel Genes in Patients With Metastatic Breast Cancer -Association With Patient and Disease Characteristics and Effect on Prognosis" (2021) in Journal of Clinical Oncology

The scientist frequently collaborates with multiple researchers, with the most frequent co-authors being:

  • Matthias Schmid
  • Arif B. Ekici
  • Cornelia Kraus
  • Kai-Uwe Eckardt
  • Christiane Zweier

Best Publications

  • Correction: Corrigendum: Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis

    John Bowes;Ashley Budu-Aggrey;Ulrike Huffmeier;Steffen Uebe

  • Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

    Robyn H. Wallace;Dao W. Wang;Rita Singh;Rita Singh;Ingrid E. Scheffer;Ingrid E. Scheffer;Ingrid E. Scheffer

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

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

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

    Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland

  • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Lam C. Tsoi;Sarah L. Spain;Sarah L. Spain;Jo Knight;Eva Ellinghaus;Eva Ellinghaus

  • A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1

    Amy Strange;Francesca Capon;Chris C A Spencer

  • Genome-wide, large-scale production of mutant mice by ENU mutagenesis

    M. H. Hrabe de Angelis;H. Flaswinkel;H. Fuchs;B. Rathkolb

  • Psoriasis is associated with increased beta-defensin genomic copy number.

    Edward J Hollox;Ulrike Huffmeier;Patrick L J M Zeeuwen;Raquel Palla

  • Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.

    Sabine Endele;Georg Rosenberger;Kirsten Geider;Bernt Popp

  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

    Sébastien Jacquemont;Alexandre Reymond;Flore Zufferey;Louise Harewood

  • Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases A Mendelian Randomization Study

    Philip C Haycock;Stephen Burgess;Aayah Nounu

  • Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

    Anita Rauch;Juliane Hoyer;Sabine Guth;Christiane Zweier

  • Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

    Martin Zenker;Thomas Aigner;Olaf Wendler;Tim Tralau

  • A comprehensive linkage analysis for myocardial infarction and its related risk factors.

    Ulrich Broeckel;Christian Hengstenberg;Björn Mayer;Stephan Holmer

  • Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation

    Francesca Pasutto;Heinrich Sticht;Gerhard Hammersen;Gabriele Gillessen-Kaesbach

  • Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huet anomaly)

    Katrin Hoffmann;Katrin Hoffmann;Christine K. Dreger;Ada L. Olins;Donald E. Olins

  • Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

    Anita Rauch;Christian T. Thiel;Detlev Schindler;Ursula Wick

  • A Genome-wide Search for Linkage to Asthma

    Matthias Wjst;Guido Fischer;Thomas Immervoll;Martin Jung

  • A genome-wide asociation study identifies new psoriasis susceptibility loci and an interaction betwEn HLA-C and ERAP1

    A. Strange;F. Capon;C. C. A. Spencer;J. Knight

  • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    L. C. Tsoi;S. L. Spain;J. Knight;E. Ellinghaus

Frequent Co-Authors

Arif B. Ekici
Arif B. Ekici University of Erlangen-Nuremberg
Anita Rauch
Anita Rauch University of Zurich
Christiane Zweier
Christiane Zweier University of Erlangen-Nuremberg
Heinrich Sticht
Heinrich Sticht University of Erlangen-Nuremberg
Thomas F. Wienker
Thomas F. Wienker Max Planck Society
Hans Christian Hennies
Hans Christian Hennies University of Huddersfield
Rami Abou Jamra
Rami Abou Jamra Leipzig University
Martin Zenker
Martin Zenker Otto-von-Guericke University Magdeburg
Kathrin Saar
Kathrin Saar Max Delbrück Center for Molecular Medicine
Franz Rüschendorf
Franz Rüschendorf Max Delbrück Center for Molecular Medicine

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