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Sugirthan Sivalingam

Showing results (21-30 of 32) with videos related to

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Molecular Autism|June 25, 2020
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational studyAxel Krug, Markus Wöhr, Dominik Seffer, et al.
Plos One|November 1, 2018
Exome sequencing in large, multiplex bipolar disorder families from CubaAnna Maaser, Andreas J Forstner, Jana Strohmaier, et al.
American Journal of Human Genetics|June 5, 2020
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP SyndromeHuijun Wang, Aytaj Humbatova, Yuanxiang Liu, et al.
European Journal of Human Genetics : EJHG|November 2, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformationsJulia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, et al.
Nature|July 23, 2025
Structural variation in 1,019 diverse humans based on long-read sequencingSiegfried Schloissnig, Samarendra Pani, Jana Ebler, et al.
Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
International Journal of Bipolar Disorders|February 13, 2020
The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorderAshley L Comes, Darina Czamara, Kristina Adorjan, et al.
Translational Psychiatry|February 19, 2020
Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder familiesAndreas J Forstner, Sascha B Fischer, Lorena M Schenk, et al.
Nature Genetics|February 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptorsTzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, et al.
Plos One|February 7, 2017
Identification of shared risk loci and pathways for bipolar disorder and schizophreniaAndreas J Forstner, Julian Hecker, Andrea Hofmann, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Molecular Autism|June 25, 2020
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational studyAxel Krug, Markus Wöhr, Dominik Seffer, et al.
Plos One|November 1, 2018
Exome sequencing in large, multiplex bipolar disorder families from CubaAnna Maaser, Andreas J Forstner, Jana Strohmaier, et al.
American Journal of Human Genetics|June 5, 2020
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP SyndromeHuijun Wang, Aytaj Humbatova, Yuanxiang Liu, et al.
European Journal of Human Genetics : EJHG|November 2, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformationsJulia Fabian, Gabriel C Dworschak, Lea Waffenschmidt, et al.
Nature|July 23, 2025
Structural variation in 1,019 diverse humans based on long-read sequencingSiegfried Schloissnig, Samarendra Pani, Jana Ebler, et al.
Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
International Journal of Bipolar Disorders|February 13, 2020
The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorderAshley L Comes, Darina Czamara, Kristina Adorjan, et al.
Translational Psychiatry|February 19, 2020
Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder familiesAndreas J Forstner, Sascha B Fischer, Lorena M Schenk, et al.
Nature Genetics|February 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptorsTzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa, et al.
Plos One|February 7, 2017
Identification of shared risk loci and pathways for bipolar disorder and schizophreniaAndreas J Forstner, Julian Hecker, Andrea Hofmann, et al.
Pageof 4