Jens Michael Hertz

X-linked Alport Syndrome

Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras et al. · Journal of the American Society of Nephrology · 2000 · 595 citations

Life Sciences, Genetics, Molecular Genetics +16

X-Linked Alport Syndrome

Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras et al. · Journal of the American Society of Nephrology · 2003 · 481 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Transcriptional regulator PRDM12 is essential for human pain perception

Ya-Chun Chen, Michaela Auer‐Grumbach, Shinya Matsukawa et al. · Nature Genetics · 2015 · 173 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +12

Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2

Erik‐Jan Kamsteeg, Claudio Catalli, Jens Michael Hertz et al. · European Journal of Human Genetics · 2012 · 163 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient.

Jingbin Zhou, Jens Michael Hertz, Anu Leinonen et al. · Journal of Biological Chemistry · 1992 · 148 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14