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Delnaz Roshandel

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Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum DisorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Plos One|December 2, 2011
Polymorphisms in genes involved in the NF-κB signalling pathway are associated with bone mineral density, geometry and turnover in menDelnaz Roshandel, Wendy Thomson, Stephen R Pye, et al.
Calcified Tissue International|October 4, 2011
Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in menDelnaz Roshandel, Kate L Holliday, Stephen R Pye, et al.
BMC Medical Genetics|February 1, 2011
A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing StudyDelnaz Roshandel, Wendy Thomson, Stephen R Pye, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 6, 2010
Genetic variation in the RANKL/RANK/OPG signaling pathway is associated with bone turnover and bone mineral density in menDelnaz Roshandel, Kate L Holliday, Stephen R Pye, et al.
Diabetes|May 22, 2016
New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated ProteinsDelnaz Roshandel, Ronald Klein, Barbara E K Klein, et al.
Arthritis and Rheumatism|June 7, 2013
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysisGang Xie, Delnaz Roshandel, Richard Sherva, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
NPJ Genomic Medicine|September 28, 2023
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsyDelnaz Roshandel, Eric J Sanders, Amy Shakeshaft, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum DisorderMarla Mendes, Desmond Zeya Chen, Worrawat Engchuan, et al.
Plos One|December 2, 2011
Polymorphisms in genes involved in the NF-κB signalling pathway are associated with bone mineral density, geometry and turnover in menDelnaz Roshandel, Wendy Thomson, Stephen R Pye, et al.
Calcified Tissue International|October 4, 2011
Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in menDelnaz Roshandel, Kate L Holliday, Stephen R Pye, et al.
BMC Medical Genetics|February 1, 2011
A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing StudyDelnaz Roshandel, Wendy Thomson, Stephen R Pye, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 6, 2010
Genetic variation in the RANKL/RANK/OPG signaling pathway is associated with bone turnover and bone mineral density in menDelnaz Roshandel, Kate L Holliday, Stephen R Pye, et al.
Diabetes|May 22, 2016
New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated ProteinsDelnaz Roshandel, Ronald Klein, Barbara E K Klein, et al.
Arthritis and Rheumatism|June 7, 2013
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysisGang Xie, Delnaz Roshandel, Richard Sherva, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
NPJ Genomic Medicine|September 28, 2023
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsyDelnaz Roshandel, Eric J Sanders, Amy Shakeshaft, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
Pageof 4