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Martin Kircher

Showing results (51-60 of 89) with videos related to

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Biorxiv : the Preprint Server for Biology|March 22, 2023
Massively parallel characterization of transcriptional regulatory elements in three diverse human cell typesVikram Agarwal, Fumitaka Inoue, Max Schubach, et al.
American Journal of Human Genetics|January 16, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learningSaranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
American Journal of Human Genetics|March 8, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learningSaranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
Human Molecular Genetics|November 13, 2013
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complexMarie Estelle Losfeld, Bobby G Ng, Martin Kircher, et al.
Cancer Discovery|December 5, 2014
Biallelic mutations in BRCA1 cause a new Fanconi anemia subtypeSarah L Sawyer, Lei Tian, Marketta Kähkönen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 4, 2012
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewalSimone A Fietz, Robert Lachmann, Holger Brandl, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
American Journal of Human Genetics|September 28, 2011
Denisova admixture and the first modern human dispersals into Southeast Asia and OceaniaDavid Reich, Nick Patterson, Martin Kircher, et al.
Blood Advances|January 4, 2018
Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiativeJill M Johnsen, Shelley N Fletcher, Haley Huston, et al.
Journal of Thrombosis and Haemostasis : JTH|June 30, 2022
Results of genetic analysis of 11 341 participants enrolled in the My Life, Our Future hemophilia genotyping initiative in the United StatesJill M Johnsen, Shelley N Fletcher, Angela Dove, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Biorxiv : the Preprint Server for Biology|March 22, 2023
Massively parallel characterization of transcriptional regulatory elements in three diverse human cell typesVikram Agarwal, Fumitaka Inoue, Max Schubach, et al.
American Journal of Human Genetics|January 16, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learningSaranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
American Journal of Human Genetics|March 8, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learningSaranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
Human Molecular Genetics|November 13, 2013
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complexMarie Estelle Losfeld, Bobby G Ng, Martin Kircher, et al.
Cancer Discovery|December 5, 2014
Biallelic mutations in BRCA1 cause a new Fanconi anemia subtypeSarah L Sawyer, Lei Tian, Marketta Kähkönen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 4, 2012
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewalSimone A Fietz, Robert Lachmann, Holger Brandl, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
American Journal of Human Genetics|September 28, 2011
Denisova admixture and the first modern human dispersals into Southeast Asia and OceaniaDavid Reich, Nick Patterson, Martin Kircher, et al.
Blood Advances|January 4, 2018
Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiativeJill M Johnsen, Shelley N Fletcher, Haley Huston, et al.
Journal of Thrombosis and Haemostasis : JTH|June 30, 2022
Results of genetic analysis of 11 341 participants enrolled in the My Life, Our Future hemophilia genotyping initiative in the United StatesJill M Johnsen, Shelley N Fletcher, Angela Dove, et al.
Pageof 9