Association study of the three functional polymorphisms (TAS2R46G>A, OR4C16G>A, and OR4X1A>T) with recurrent pregnancy loss-Reference-Cited by-同舟云学术

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Association study of the three functional polymorphisms (TAS2R46G>A, OR4C16G>A, and OR4X1A>T) with recurrent pregnancy loss

Published:2018-09-10 Issue:1 Volume:41 Page:61-70
ISSN:1976-9571
Container-title:Genes & Genomics
language:en
Short-container-title:Genes Genom

Author:

Ryu Chang Soo,Sakong Jung Hyun,Ahn Eun Hee,Kim Jung Oh,Ko Daeun,Kim Ji Hyang,Lee Woo Sik,Kim Nam Keun

Funder

Korea Healthcare Technology R&D Project

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Link

http://link.springer.com/article/10.1007/s13258-018-0738-5/fulltext.html

Reference36 articles.

1. Abel BS, Shaw ND, Brown JM, Adams JM, Alati T, Martin KA, Pitteloud N, Seminara SB, Plummer L, Pignatelli D et al (2013) Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism. J Clin Endocrinol Metab 98:E206–E216

2. Ahn YJ, Markkandan K, Baek IP, Mun S, Lee W, Kim HS, Han K (2018) An efficient and tunable parameter to improve variant calling for whole genome and exome sequencing data. Genes Genom 40:39–47

3. Benjamini Y, Drai D, Elmer G, Kafkafi N, Golani I (2001) Controlling the false discovery rate in behavior genetics research. Behav Brain Res 125:279–284

4. Bhuiyan ZA, Momenah TS, Gong Q, Amin AS, Ghamdi SA, Carvalho JS, Homfray T, Mannens MM, Zhou Z, Wilde AA et al (2008) Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation. Heart Rhythm 5:553–561

5. Bondeson ML, Ericson K, Gudmundsson S, Ameur A, Ponten F, Wesstrom J, Frykholm C, Wilbe M (2017) A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy. Clin Genet 92:510–516

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2. Association of Polymorphisms in FSHR, INHA, ESR1, and BMP15 with Recurrent Implantation Failure;Biomedicines;2023-05-05

3. Association of Polymorphisms in the Long Non-Coding RNA HOTAIR with Recurrent Pregnancy Loss in a Korean Population;Genes;2022-11-17

4. Genetic Variations miR-10aA>T, miR-30cA>G, miR-181aT>C, and miR-499bA>G and the Risk of Recurrent Pregnancy Loss in Korean Women;Biomedicines;2022-09-25

5. Role of miRNA polymorphism in recurrent pregnancy loss: a systematic review and meta-analysis;Biomarkers in Medicine;2022-02

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