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Milan Hiersche

Showing results (1-10 of 6) with videos related to

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Plos One|August 27, 2013
Postgwas: advanced GWAS interpretation in RMilan Hiersche, Frank Rühle, Monika Stoll
Blood|September 20, 2012
A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric strokeAstrid Arning, Milan Hiersche, Anika Witten, et al.
Human Genomics|June 11, 2026
An example for potentially underrated causes of recessive disease in the Greater Middle East: integrative long-read genome and transcriptome sequencing pinpoint a deep-intronic homozygous HEXB candidate founder variant in GM2-gangliosidosisAngelika Bolte, Clara Velmans, Christian Netzer, et al.
Plos One|February 4, 2015
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney diseaseTobias Eisenberger, Christian Decker, Milan Hiersche, et al.
Blood|December 25, 2016
Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolismFrank Rühle, Anika Witten, Andrei Barysenka, et al.
Nature Genetics|May 23, 2017
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseHao Lu, Maria C Rondón Galeano, Elisabeth Ott, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Plos One|August 27, 2013
Postgwas: advanced GWAS interpretation in RMilan Hiersche, Frank Rühle, Monika Stoll
Blood|September 20, 2012
A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric strokeAstrid Arning, Milan Hiersche, Anika Witten, et al.
Human Genomics|June 11, 2026
An example for potentially underrated causes of recessive disease in the Greater Middle East: integrative long-read genome and transcriptome sequencing pinpoint a deep-intronic homozygous HEXB candidate founder variant in GM2-gangliosidosisAngelika Bolte, Clara Velmans, Christian Netzer, et al.
Plos One|February 4, 2015
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney diseaseTobias Eisenberger, Christian Decker, Milan Hiersche, et al.
Blood|December 25, 2016
Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolismFrank Rühle, Anika Witten, Andrei Barysenka, et al.
Nature Genetics|May 23, 2017
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseHao Lu, Maria C Rondón Galeano, Elisabeth Ott, et al.
Pageof 1