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Genetics

D-Index
61
Citations
12943
World Ranking
3066
National Ranking
211

Overview

Jochen Graw is affiliated with the Technical University of Munich in Germany. Their research primarily focuses on the fields of Biochemistry, Genetics and Molecular Biology, with a strong emphasis on subfields including Molecular Biology, Genetics, Ophthalmology, Radiology, Nuclear Medicine and Imaging, and Aging.

The scientist's work covers several main topics, notably:

  • Connexins and lens biology
  • Retinal Development and Disorders
  • S100 Proteins and Annexins
  • Genetics, Aging, and Longevity in Model Organisms
  • Adipose Tissue and Metabolism
  • Retinal Diseases and Treatments
  • Advanced biosensing and bioanalysis techniques

Among the recent papers associated with Jochen Graw are:

  • Imbalances in the eye lens proteome are linked to cataract formation, 2021, Nature Structural & Molecular Biology
  • Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice, 2022, Nature Communications
  • A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes, 2020, Mammalian Genome
  • Dose-dependent long-term effects of a single radiation event on behaviour and glial cells, 2020, International Journal of Radiation Biology
  • Genome-wide screening reveals the genetic basis of mammalian embryonic eye development, 2023, BMC Biology

Frequent co-authors who have collaborated with Jochen Graw include:

  • Henning Hintzsche
  • Martin Hrabé de Angelis
  • Helmut Fuchs
  • Sabine M. Hölter
  • Oana V. Amarie

Publication venues where Jochen Graw's work frequently appears include:

  • BIOspektrum
  • International Journal of Radiation Biology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Experimental Eye Research
  • Nature Structural & Molecular Biology

Best Publications

  • A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

    Wolfgang Enard;Sabine Gehre;Kurt Hammerschmidt;Sabine M. Hölter

  • Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.

    Natalia S. Pellegata;Leticia Quintanilla-Martinez;Heide Siggelkow;Elenore Samson

  • A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

    Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs

  • Radiation cataractogenesis: a review of recent studies.

    E. A. Ainsbury;S. D. Bouffler;W. Dörr;J. Graw

  • Rapamycin extends murine lifespan but has limited effects on aging

    Frauke Neff;Diana Flores-Dominguez;Devon P. Ryan;Marion Horsch

  • Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3.

    Marten P. Smidt;Simone M. Smits;Hans Bouwmeester;Frank P. T. Hamers

  • Genetics of crystallins: cataract and beyond.

    Jochen Graw

  • The genetic and molecular basis of congenital eye defects

    Jochen Graw

  • Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice

    Elena V. Semina;Jeffrey C. Murray;Rebecca Reiter;Ronald F. Hrstka

  • Prevalence of sexual dimorphism in mammalian phenotypic traits

    Natasha A. Karp;Natasha A. Karp;Jeremy Mason;Arthur L. Beaudet;Yoav Benjamini

  • Haemophilia A: from mutation analysis to new therapies

    Jochen Graw;Hans-Hermann Brackmann;Johannes Oldenburg;Reinhard Schneppenheim

  • The crystallins: genes, proteins and diseases.

    Graw J

  • Introducing the German Mouse Clinic: open access platform for standardized phenotyping

    Valérie Gailus-Durner;Helmut Fuchs;Lore Becker;Ines Bolle

  • Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development

    Nicole Haubst;Joachim Berger;Venugopal Radjendirane;Jochen Graw

  • Genetic Aspects of Embryonic Eye Development in Vertebrates

    Jochen Graw

  • Congenital hereditary cataracts

    Jochen Graw

  • Altered aggregation properties of mutant γ-crystallins cause inherited cataract

    Aileen Sandilands;Aileen M. Hutcheson;Heather A. Long;Alan R. Prescott

  • Ionizing radiation induced cataracts: Recent biological and mechanistic developments and perspectives for future research.

    Elizabeth A. Ainsbury;Stephen Barnard;Scott Bright;Claudia Dalke

  • Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.

    Martin Hrabě de Angelis;George Nicholson;Mohammed Selloum;Jacqueline K White

  • A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

    Michael R. Bowl;Michelle M. Simon;Neil J. Ingham;Neil J. Ingham;Simon Greenaway

Frequent Co-Authors

Eckhard Wolf
Eckhard Wolf Ludwig-Maximilians-Universität München
Helmut Fuchs
Helmut Fuchs Helmholtz Zentrum München
Valerie Gailus-Durner
Valerie Gailus-Durner Helmholtz Zentrum München
Martin Hrabé de Angelis
Martin Hrabé de Angelis Technical University of Munich
Wolfgang Wurst
Wolfgang Wurst German Center for Neurodegenerative Diseases
Martin Klingenspor
Martin Klingenspor Technical University of Munich
Dirk H. Busch
Dirk H. Busch Technical University of Munich
Thomas Klopstock
Thomas Klopstock Ludwig-Maximilians-Universität München
Jerzy Adamski
Jerzy Adamski Helmholtz Association of German Research Centres
Johannes Beckers
Johannes Beckers Technical University of Munich

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