Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Najeeb Syed

Showing results (1-10 of 47) with videos related to

Pageof 5
Sort By:
Clinical Case Reports|December 23, 2021
Maturity-onset diabetes of the young (MODY) due to PDX1 mutation in a sib-pair diabetes family from QatarBasma Haris, Idris Mohammed, Najeeb Syed, et al.
Human Genomics|October 8, 2021
Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari populationShaza Malik, Roan Zaied, Najeeb Syed, et al.
Human Mutation|August 24, 2021
Actionable genomic variants in 6045 participants from the Qatar Genome ProgramAmal Elfatih, Borbala Mifsud, Najeeb Syed, et al.
Scientific Reports|August 24, 2017
Accelerating next generation sequencing data analysis with system level optimizationsNagarajan Kathiresan, Ramzi Temanni, Hakeem Almabrazi, et al.
Obesity Facts|January 13, 2022
The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in QatarNadien AbouHashem, Roan E Zaied, Kholoud Al-Shafai, et al.
Scientific Reports|February 1, 2017
Genome-wide Regulatory Roles of the C2H2-type Zinc Finger Protein ZNF764 on the Glucocorticoid ReceptorAbeer Fadda, Najeeb Syed, Rafah Mackeh, et al.
Journal of the Endocrine Society|January 31, 2018
Single-Nucleotide Variations of the Human Nuclear Hormone Receptor Genes in 60,000 IndividualsRafah Mackeh, Alexandra K Marr, Soha R Dargham, et al.
Journal of Personalized Medicine|January 12, 2021
A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank CohortNadin Younes, Najeeb Syed, Santosh K Yadav, et al.
The Journal of Gene Medicine|August 28, 2023
A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertilityShoaib Nawaz, Shabir Hussain, Muhammad Bilal, et al.
Aging|November 21, 2019
Association of genes with phenotype in autism spectrum disorderSabah Nisar, Sheema Hashem, Ajaz A Bhat, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Clinical Case Reports|December 23, 2021
Maturity-onset diabetes of the young (MODY) due to PDX1 mutation in a sib-pair diabetes family from QatarBasma Haris, Idris Mohammed, Najeeb Syed, et al.
Human Genomics|October 8, 2021
Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari populationShaza Malik, Roan Zaied, Najeeb Syed, et al.
Human Mutation|August 24, 2021
Actionable genomic variants in 6045 participants from the Qatar Genome ProgramAmal Elfatih, Borbala Mifsud, Najeeb Syed, et al.
Scientific Reports|August 24, 2017
Accelerating next generation sequencing data analysis with system level optimizationsNagarajan Kathiresan, Ramzi Temanni, Hakeem Almabrazi, et al.
Obesity Facts|January 13, 2022
The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in QatarNadien AbouHashem, Roan E Zaied, Kholoud Al-Shafai, et al.
Scientific Reports|February 1, 2017
Genome-wide Regulatory Roles of the C2H2-type Zinc Finger Protein ZNF764 on the Glucocorticoid ReceptorAbeer Fadda, Najeeb Syed, Rafah Mackeh, et al.
Journal of the Endocrine Society|January 31, 2018
Single-Nucleotide Variations of the Human Nuclear Hormone Receptor Genes in 60,000 IndividualsRafah Mackeh, Alexandra K Marr, Soha R Dargham, et al.
Journal of Personalized Medicine|January 12, 2021
A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank CohortNadin Younes, Najeeb Syed, Santosh K Yadav, et al.
The Journal of Gene Medicine|August 28, 2023
A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertilityShoaib Nawaz, Shabir Hussain, Muhammad Bilal, et al.
Aging|November 21, 2019
Association of genes with phenotype in autism spectrum disorderSabah Nisar, Sheema Hashem, Ajaz A Bhat, et al.
Pageof 5