Mohammad R. Toliat - Cologne Center for Genomics, Institute for Genetics, University of Cologne, Weyertal 115b, 50931 Köln, Germany

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论文共 65 篇作者统计合作学者相似作者

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cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNA

Florian Erger, Deborah Nörling, Domenica Borchert, Esther Leenen,Sandra Habbig,Michael S Wiesener,Malte P Bartram,Andrea Wenzel,Christian Becker,Mohammad R Toliat,Peter Nürnberg,Bodo B Beck,

Genome Med（2020）

引用28浏览0WOS引用

Copy number variants in lipid metabolism genes are associated with gallstones disease in men

Eduardo Pérez-Palma, Bernabé I Bustos,Dennis Lal,Stephan Buch,Lorena Azocar,Mohammad Reza Toliat,Wolfgang Lieb,Andre Franke,Sebastian Hinz, Greta Burmeister, Witigo von Shönfels,Clemens Schafmayer,

EUROPEAN JOURNAL OF HUMAN GENETICS（2020）

引用4浏览0WOS引用

Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss

Birgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, Andreas Breß, Janine Altmüller, Susanne Motameny,Amit Kawalia,Holger Thiele, Kathryn Konrad,Christian Becker,Mohammad R Toliat, Gudrun Nürnberg,

CLINICAL GENETICS（2020）

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The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype

Gökhan Yigit,Ken Saida, Danielle DeMarzo,Noriko Miyake,Atsushi Fujita, Tiong Yang Tan,Susan M White, Alexandrea Wadley,Mohammad R Toliat, Susanne Motameny, Marek Franitza, Chloe A Stutterd,

HUMAN MUTATION（2020）

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Genetic Information From Discordant Sibling Pairs Points To Esrp2 As A Candidate Trans-Acting Regulator Of The Cf Modifier Gene Scnn1b

Tim Becker,Andreas Pich,Stephanie Tamm,Silke Hedtfeld, Mohammed Ibrahim,Janine Altmüller, Nina Dalibor,Mohammad Reza Toliat, Sabina Janciauskiene,Burkhard Tümmler,Frauke Stanke

SCIENTIFIC REPORTS（2020）

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Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration

Felix Grassmann, Sebastian Harsch,Caroline Brandl,Christina Kiel,Peter Nürnberg,Mohammad R Toliat,Monika Fleckenstein,Maximilian Pfau,Steffen Schmitz-Valckenberg,Frank G Holz,Emily Y Chew,Anand Swaroop,

JAMA OPHTHALMOLOGY（2019）

引用25浏览0WOS引用

Qualitative and Quantitative Analysis of IDH1 Mutation in Progressive Gliomas by Allele-Specific qPCR and Western Blot Analysis

Moritz Perrech, Lena Dreher,Gabriele Röhn, Pantelis Stavrinou,Boris Krischek,Mohammad Toliat,Roland Goldbrunner, Marco Timmer

TECHNOLOGY IN CANCER RESEARCH & TREATMENT（2019）

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Biallelic mutation of human SLC6A6 encoding the taurine transporter TAUT is linked to early retinal degeneration

Markus N Preising, Boris Görg,Christoph Friedburg,Natalia Qvartskhava, Birgit S Budde,Michele Bonus,Mohammad R Toliat,Christopher Pfleger, Janine Altmüller, Diran Herebian, Mila Beyer,Helge J Zöllner,

FASEB JOURNAL（2019）

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Variants In Abcg8 And Traf3 Genes Confer Risk For Gallstone Disease In Admixed Latinos With Mapuche Native American Ancestry

Bernabé I Bustos,Eduardo Pérez-Palma,Stephan Buch,Lorena Azócar,Eleodoro Riveras,Giorgia D Ugarte,Mohammad Toliat,Peter Nürnberg,Wolfgang Lieb,Andre Franke,Sebastian Hinz, Greta Burmeister,

SCIENTIFIC REPORTS（2019）

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Common variants in ABCG8 and TRAF3 genes confer risk for gallstone disease and gallbladder cancer in admixed Latinos with Mapuche Native American ancestry

Bernabé I. Bustos,Eduardo Pérez-Palma,Stephan Buch,Lorena Azocar,Eleodoro Riveras,Giorgia D. Ugarte,Mohammad R. Toliat,Peter Nuernberg,Wolfgang Lieb,Andre Franke,Sebastian Hinz, Greta Burmeister,

bioRxiv（2018）

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