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Denny Popp

Showing results (31-40 of 35) with videos related to

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International Journal of Obesity (2005)|June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individualsRobert Künzel, Helene Faust, Linnaeus Bundalian, et al.
NAR Genomics and Bioinformatics|January 19, 2026
SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genomeLinnaeus Bundalian, Martina Schmidt Strnadová, Felix Garten, et al.
Frontiers in Cell and Developmental Biology|February 2, 2023
<i>PHIP</i>-associated Chung-Jansen syndrome: Report of 23 new individualsAntje Kampmeier, Elsa Leitão, Ilaria Parenti, et al.
American Journal of Human Genetics|July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth diseaseDaniel G Calame, Tianyu Guo, Chen Wang, et al.
The New England Journal of Medicine|June 5, 2024
Genome Sequencing for Diagnosing Rare DiseasesMonica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
International Journal of Obesity (2005)|June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individualsRobert Künzel, Helene Faust, Linnaeus Bundalian, et al.
NAR Genomics and Bioinformatics|January 19, 2026
SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genomeLinnaeus Bundalian, Martina Schmidt Strnadová, Felix Garten, et al.
Frontiers in Cell and Developmental Biology|February 2, 2023
<i>PHIP</i>-associated Chung-Jansen syndrome: Report of 23 new individualsAntje Kampmeier, Elsa Leitão, Ilaria Parenti, et al.
American Journal of Human Genetics|July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth diseaseDaniel G Calame, Tianyu Guo, Chen Wang, et al.
The New England Journal of Medicine|June 5, 2024
Genome Sequencing for Diagnosing Rare DiseasesMonica H Wojcik, Gabrielle Lemire, Eva Berger, et al.
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