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Adam Ameur

Showing results (81-90 of 103) with videos related to

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Communications Biology|November 20, 2025
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomesAnne-Mai Ilumäe, Helen Post, Rodrigo Flores, et al.
Scientific Reports|June 9, 2017
SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclastsEva-Lena Stattin, Petra Henning, Joakim Klar, et al.
G3 (Bethesda, Md.)|May 22, 2016
Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland PoniesNima Rafati, Lisa S Andersson, Sofia Mikko, et al.
European Journal of Human Genetics : EJHG|August 4, 2011
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traitsGhazal Zaboli, Adam Ameur, Wilmar Igl, et al.
Journal of Medical Genetics|January 8, 2016
Identification of novel genetic causes of Rett syndrome-like phenotypesFátima Lopes, Mafalda Barbosa, Adam Ameur, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversionsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse Bengtsson, et al.
BMC Research Notes|October 11, 2023
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REHMariya Lysenkova Wiklander, Elin Övernäs, Johanna Lagensjö, et al.
Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Nature Communications|January 6, 2022
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophreniaMatthew Halvorsen, Ruth Huh, Nikolay Oskolkov, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Communications Biology|November 20, 2025
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomesAnne-Mai Ilumäe, Helen Post, Rodrigo Flores, et al.
Scientific Reports|June 9, 2017
SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclastsEva-Lena Stattin, Petra Henning, Joakim Klar, et al.
G3 (Bethesda, Md.)|May 22, 2016
Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland PoniesNima Rafati, Lisa S Andersson, Sofia Mikko, et al.
European Journal of Human Genetics : EJHG|August 4, 2011
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traitsGhazal Zaboli, Adam Ameur, Wilmar Igl, et al.
Journal of Medical Genetics|January 8, 2016
Identification of novel genetic causes of Rett syndrome-like phenotypesFátima Lopes, Mafalda Barbosa, Adam Ameur, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversionsKristine Bilgrav Saether, Jesper Eisfeldt, Jesse Bengtsson, et al.
BMC Research Notes|October 11, 2023
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REHMariya Lysenkova Wiklander, Elin Övernäs, Johanna Lagensjö, et al.
Human Molecular Genetics|October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysAlvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Nature Communications|January 6, 2022
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophreniaMatthew Halvorsen, Ruth Huh, Nikolay Oskolkov, et al.
Pageof 11