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Jamil Ahmad

Showing results (231-240 of 260) with videos related to

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Molecular Biology Reports|January 7, 2014
Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan originAbdul Hameed Baloch, Shakeela Daud, Nafeesa Raheem, et al.
Molecular Genetics & Genomic Medicine|January 3, 2019
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and PakistanDulce Lima Cunha, Omar Mohammed Alakloby, Robert Gruber, et al.
Plastic and Reconstructive Surgery|November 25, 2020
Evidence-Based Performance Measures for Rhinoplasty: A Multidisciplinary Performance Measure SetMichele A Manahan, Fred Fedok, Caryn Davidson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2025
Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic ParaplegiaRui Zhu, Lang Liu, Mehrdad A Estiar, et al.
NPJ Parkinson'S Disease|October 25, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
Are rare heterozygous <i>SYNJ1</i> variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Brain : a Journal of Neurology|March 12, 2014
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthoodJoanne Ng, Juan Zhen, Esther Meyer, et al.
Pageof 26

Showing results (231-240 of 260) with videos related to

Sort By:
Pageof 26
Molecular Biology Reports|January 7, 2014
Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan originAbdul Hameed Baloch, Shakeela Daud, Nafeesa Raheem, et al.
Molecular Genetics & Genomic Medicine|January 3, 2019
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and PakistanDulce Lima Cunha, Omar Mohammed Alakloby, Robert Gruber, et al.
Plastic and Reconstructive Surgery|November 25, 2020
Evidence-Based Performance Measures for Rhinoplasty: A Multidisciplinary Performance Measure SetMichele A Manahan, Fred Fedok, Caryn Davidson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2025
Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic ParaplegiaRui Zhu, Lang Liu, Mehrdad A Estiar, et al.
NPJ Parkinson'S Disease|October 25, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
Are rare heterozygous <i>SYNJ1</i> variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Brain : a Journal of Neurology|March 12, 2014
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthoodJoanne Ng, Juan Zhen, Esther Meyer, et al.
Pageof 26