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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Anovulation and LHCGR[original query]
Genotype-phenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large cohort of Han Chinese women.
Human reproduction (Oxford, England) 2012 Dec .
Cui L, Zhao H, Zhang B, Qu Z, Liu J, Liang X, Zhao X, Zhao J, Sun Y, Wang P, Li T, Shi Y, Chen ZJ
Association of luteinizing hormone chorionic gonadotropin receptor gene polymorphism (rs2293275) with polycystic ovarian syndrome.
Genetic testing and molecular biomarkers 2015 Mar 19 (3): 128-32.
Thathapudi Sujatha, Kodati Vijayalakshmi, Erukkambattu Jayashankar, Addepally Uma, Qurratulain Has
Polycystic ovary syndrome susceptibility single nucleotide polymorphisms in women with a single PCOS clinical feature.
Human reproduction (Oxford, England) 2015 Mar 30 (3): 732-6.
Cui Linlin, Li Guangyu, Zhong Wanxia, Bian Yuehong, Su Shizhen, Sheng Yan, Shi Yuhua, Wei Daimin, Zhang Wei, Zhao Han, Chen Zi-Jia
Pooled genetic analysis identifies variants that confer enhanced susceptibility to PCOS in Indian ethnicity.
Gene 2020 May 144760.
Vishnubotla Deepa Switha, Shek Aaji Pasha, Madireddi Sujat
A Comprehensive Overview of Common Polymorphic Variants in Genes Related to Polycystic Ovary Syndrome.
Reproductive sciences (Thousand Oaks, Calif.) 2020 Nov .
Castillo-Higuera Tatiana, Alarcón-Granados María Camila, Marin-Suarez Johana, Moreno-Ortiz Harold, Esteban-Pérez Clara Inés, Ferrebuz-Cardozo Atilio Junior, Forero-Castro Maribel, Camargo-Vill Alba Glor
Pilot study on evaluation and determination of the prevalence of Polycystic Ovarian Syndrome (PCOS) associated gene markers in the South Indian population.
Indian journal of endocrinology and metabolism 2022 3 25 (6): 551-558.
Ramanathan Balaji, Murugan Jeyasudha, Velayutham Kumarav
A Case-Control Study of the Luteinizing Hormone Level in Luteinizing Hormone Receptor Gene (rs2293275) Polymorphism in Polycystic Ovarian Syndrome Females.
Public health genomics 2022 3 1-9.
Atoum Manar Fayiz, Alajlouni Mai Mahamad, Alzoughool Fo
Whole exome sequencing identifies a novel homozygous missense mutation of LHCGR gene in primary infertile women with empty follicle syndrome.
The journal of obstetrics and gynaecology research 2023 7 .
Yang Xu, Enhua Wang, Tianfeng Liu, Surong Wang, Fengxia Wu, Xiangyu Zhao, Ancong Wa
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