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L Wiggs

Showing results (181-190 of 296) with videos related to

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Ophthalmology. Glaucoma|June 2, 2026
Primary Open Angle Glaucoma Polygenic Risk Score is Associated with Disease ProgressionNiloufar Bineshfar, Kanza Aziz, Hetince Zhao, et al.
Ophthalmology. Glaucoma|June 12, 2022
The Association of Female Reproductive Factors with Glaucoma and Related Traits: A Systematic ReviewKian M Madjedi, Kelsey V Stuart, Sharon Y L Chua, et al.
Investigative Ophthalmology & Visual Science|November 3, 2015
Nailfold Capillary Abnormalities in Primary Open-Angle Glaucoma: A Multisite StudyLouis R Pasquale, Akiko Hanyuda, Ai Ren, et al.
BMC Medicine|May 11, 2017
Habitual coffee consumption and genetic predisposition to obesity: gene-diet interaction analyses in three US prospective studiesTiange Wang, Tao Huang, Jae H Kang, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Early adult-onset POAG linked to 15q11-13 using ordered subset analysisR Rand Allingham, Janey L Wiggs, Elizabeth R Hauser, et al.
Human Molecular Genetics|August 30, 2011
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USAJaney L Wiggs, Jae Hee Kang, Brian L Yaspan, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locusLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|April 13, 2025
Genetic Risk for Open-Angle Glaucoma Subtypes Is Associated with Specific Visual Field Defect ClassesSayuri Sekimitsu, Kavin Selvan, Yan Zhao, et al.
European Journal of Human Genetics : EJHG|March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndromeLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Pageof 30

Showing results (181-190 of 296) with videos related to

Sort By:
Pageof 30
Ophthalmology. Glaucoma|June 2, 2026
Primary Open Angle Glaucoma Polygenic Risk Score is Associated with Disease ProgressionNiloufar Bineshfar, Kanza Aziz, Hetince Zhao, et al.
Ophthalmology. Glaucoma|June 12, 2022
The Association of Female Reproductive Factors with Glaucoma and Related Traits: A Systematic ReviewKian M Madjedi, Kelsey V Stuart, Sharon Y L Chua, et al.
Investigative Ophthalmology & Visual Science|November 3, 2015
Nailfold Capillary Abnormalities in Primary Open-Angle Glaucoma: A Multisite StudyLouis R Pasquale, Akiko Hanyuda, Ai Ren, et al.
BMC Medicine|May 11, 2017
Habitual coffee consumption and genetic predisposition to obesity: gene-diet interaction analyses in three US prospective studiesTiange Wang, Tao Huang, Jae H Kang, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Early adult-onset POAG linked to 15q11-13 using ordered subset analysisR Rand Allingham, Janey L Wiggs, Elizabeth R Hauser, et al.
Human Molecular Genetics|August 30, 2011
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USAJaney L Wiggs, Jae Hee Kang, Brian L Yaspan, et al.
Plos One|October 11, 2012
The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucomaJaney L Wiggs, Alex W Hewitt, Bao Jian Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locusLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Ophthalmology|April 13, 2025
Genetic Risk for Open-Angle Glaucoma Subtypes Is Associated with Specific Visual Field Defect ClassesSayuri Sekimitsu, Kavin Selvan, Yan Zhao, et al.
European Journal of Human Genetics : EJHG|March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndromeLucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Pageof 30