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Susan Walker

Showing results (201-210 of 260) with videos related to

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Journal of Attention Disorders|July 11, 2022
Associations Between ADHD Symptoms and Maternal and Birth Outcomes: An Exploratory Analysis in a Multi-Country Cohort of Expectant MothersAja Louise Murray, Diana Taut, Adriana Baban, et al.
Journal of Neurodevelopmental Disorders|October 26, 2016
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variationMatthew J Gazzellone, Mehdi Zarrei, Christie L Burton, et al.
Clinical & Translational Immunology|May 1, 2026
High-dimensional multiomics reveals perturbations to IL-6/IL-6R axis and RUNX3 in CD4<sup>+</sup> T cells during third-trimester pregnancyJennifer R Habel, Thi H O Nguyen, Natasha de Alwis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
De novo missense variants in RAC3 cause a novel neurodevelopmental syndromeGregory Costain, Bert Callewaert, Heinz Gabriel, et al.
Neurology. Genetics|June 8, 2017
<i>ARHGEF9</i> disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.
The British Journal of Dermatology|April 28, 2025
Characterisation of the clinical and photobiological features of solar urticaria: a United Kingdom multicentre cross-sectional studyNavandeep K Thumber, Hana Elsbahi, Conn McGrath, et al.
Journal of Medical Genetics|September 26, 2024
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable accessSian Ellard, Sian Morgan, Sarah L Wynn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of FallotMiriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.
Pageof 26

Showing results (201-210 of 260) with videos related to

Sort By:
Pageof 26
Journal of Attention Disorders|July 11, 2022
Associations Between ADHD Symptoms and Maternal and Birth Outcomes: An Exploratory Analysis in a Multi-Country Cohort of Expectant MothersAja Louise Murray, Diana Taut, Adriana Baban, et al.
Journal of Neurodevelopmental Disorders|October 26, 2016
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variationMatthew J Gazzellone, Mehdi Zarrei, Christie L Burton, et al.
Clinical & Translational Immunology|May 1, 2026
High-dimensional multiomics reveals perturbations to IL-6/IL-6R axis and RUNX3 in CD4<sup>+</sup> T cells during third-trimester pregnancyJennifer R Habel, Thi H O Nguyen, Natasha de Alwis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
De novo missense variants in RAC3 cause a novel neurodevelopmental syndromeGregory Costain, Bert Callewaert, Heinz Gabriel, et al.
Neurology. Genetics|June 8, 2017
<i>ARHGEF9</i> disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.
The British Journal of Dermatology|April 28, 2025
Characterisation of the clinical and photobiological features of solar urticaria: a United Kingdom multicentre cross-sectional studyNavandeep K Thumber, Hana Elsbahi, Conn McGrath, et al.
Journal of Medical Genetics|September 26, 2024
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable accessSian Ellard, Sian Morgan, Sarah L Wynn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of FallotMiriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
Nature Communications|November 27, 2025
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypesAntonio Mollica, Safia Omer, Georgiana Forguson, et al.
Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.
Pageof 26