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Peter Krawitz

Showing results (21-30 of 101) with videos related to

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BMC Genomic Data|September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkersRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)|March 10, 2022
GenRisk: a tool for comprehensive genetic risk modelingRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 6, 2023
Prevalence and determinants of subretinal drusenoid deposits in patients' first-degree relativesMatthias M Mauschitz, Benedikt J Hochbein, Hannah Klinkhammer, et al.
Pediatric Rheumatology Online Journal|November 25, 2016
Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular courseTilmann Kallinich, Anne Thorwarth, Sae-Lim von Stuckrad, et al.
Journal of Medical Genetics|November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type AUmm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Nutrients|July 13, 2024
Beneficial Effects of Synbiotics on the Gut Microbiome in Individuals with Low Fiber Intake: Secondary Analysis of a Double-Blind, Randomized Controlled TrialAakash Mantri, Linda Klümpen, Waldemar Seel, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|June 11, 2020
Hematologist-Level Classification of Mature B-Cell Neoplasm Using Deep Learning on Multiparameter Flow Cytometry DataMax Zhao, Nanditha Mallesh, Alexander Höllein, et al.
American Journal of Medical Genetics. Part A|May 10, 2024
Next-generation phenotyping in Nigerian children with Cornelia de Lange syndromeAnnabelle Arlt, Alexej Knaus, Tzung-Chien Hsieh, et al.
Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
European Journal of Human Genetics : EJHG|November 8, 2021
Combining callers improves the detection of copy number variants from whole-genome sequencingMarie Coutelier, Manuel Holtgrewe, Marten Jäger, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
BMC Genomic Data|September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkersRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)|March 10, 2022
GenRisk: a tool for comprehensive genetic risk modelingRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 6, 2023
Prevalence and determinants of subretinal drusenoid deposits in patients' first-degree relativesMatthias M Mauschitz, Benedikt J Hochbein, Hannah Klinkhammer, et al.
Pediatric Rheumatology Online Journal|November 25, 2016
Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular courseTilmann Kallinich, Anne Thorwarth, Sae-Lim von Stuckrad, et al.
Journal of Medical Genetics|November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type AUmm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Nutrients|July 13, 2024
Beneficial Effects of Synbiotics on the Gut Microbiome in Individuals with Low Fiber Intake: Secondary Analysis of a Double-Blind, Randomized Controlled TrialAakash Mantri, Linda Klümpen, Waldemar Seel, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|June 11, 2020
Hematologist-Level Classification of Mature B-Cell Neoplasm Using Deep Learning on Multiparameter Flow Cytometry DataMax Zhao, Nanditha Mallesh, Alexander Höllein, et al.
American Journal of Medical Genetics. Part A|May 10, 2024
Next-generation phenotyping in Nigerian children with Cornelia de Lange syndromeAnnabelle Arlt, Alexej Knaus, Tzung-Chien Hsieh, et al.
Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
European Journal of Human Genetics : EJHG|November 8, 2021
Combining callers improves the detection of copy number variants from whole-genome sequencingMarie Coutelier, Manuel Holtgrewe, Marten Jäger, et al.
Pageof 11