Assisted reproductive technology: June 23-30, 2016 ▲ Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)

June 23-30, 2016






Last Updated: Jun 23, 2016

• Background of couples undergoing non-invasive prenatal testing in Japan.
  Takeda Eri et al. The journal of obstetrics and gynaecology research 2016 Jun
• [Association of rs13405728 polymorphism of LHR gene with slow ovarian response].
  Yin Qianqian, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 12 (6) 840-3
• Germ line genome editing in clinics: the approaches, objectives and global society.
  Ishii Tetsuya et al. Briefings in functional genomics 2015 Nov
• Outcomes of in vitro fertilization with preimplantation genetic diagnosis: an analysis of the Unites States Assisted Reproductive Technology Surveillance Data, 2011-2012.
  Chang Jeani et al. Fertility and sterility 2015 Nov
• Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology.
  Martin Julio et al. Fertil. Steril. 2015 Sep 3.
• Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology.
  Published on 2013 by European Society of Human GeneticsEuropean Society of Human Reproduction and EmbryologyEuropean Union Eurogentest2 Coordination Action Project
• Impact of Cystic Fibrosis Transmembrane Regulator (CFTR) gene mutations on male infertility.
  Elia Jlenia, et al. Archivio italiano di urologia, andrologia : organo ufficiale [di] Società italiana di ecografia urologica e nefrologica / Associazione ricerche in urologia 2014 9 (3) 171-4
• Infertility caused by male partners with genetic defects in Sichuan Province of China.
  Quan Q, et al. Genetics and molecular research : GMR 2013 0 (4) 6512-20
• Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy.
  Harper Joyce et al. Hum. Reprod. 2014 Aug (8) 1603-9
• Folic acid supplementation and methylenetetrahydrofolate reductase (MTHFR) gene variations in relation to in vitro fertilization pregnancy outcome.
  Murto Tiina et al. Acta Obstet Gynecol Scand 2015 Jan (1) 65-71
• Imprinting methylation errors in ART.
  Hiura Hitoshi et al. Reprod. Med. Biol. 2014 (4) 193-202
• International regulatory landscape and integration of corrective genome editing into in vitro fertilization.
  Araki Motoko et al. Reprod. Biol. Endocrinol. 2014 108
• The effect of cryopreservation on the genome of gametes and embryos: principles of cryobiology and critical appraisal of the evidence.
  Kopeika Julia et al. Hum. Reprod. Update 2015 Mar (2) 209-227
• Assisted reproductive technology and somatic morbidity in childhood: a systematic review.
  Kettner Laura Ozer et al. Fertil. Steril. 2015 Mar (3) 707-19
• Assisted reproductive technology: an overview of Cochrane reviews.
  Farquhar Cindy et al. Cochrane Database Syst Rev 2014 CD010537
• Assisted Reproductive Technology (ART) 
• CDC Key Findings: The association between assisted reproductive technology and autism spectrum disorder 
• Multiplex PCR based screening for microdeletions in azoospermia factor region of Y chromosome in azoospermic and severe oligozoospermic south Indian men.
  Suganthi Ramaswamy, et al. Iranian journal of reproductive medicine 2013 3 (3) 219-26
• [Factor V Leiden in women with repeated IVF failures].
  Ivanov P, et al. Akusherstvo i ginekologii?a 2013 0 (6) 11-4
• Association of follicle-stimulating hormone receptor polymorphisms with ovarian response in Chinese women: a prospective clinical study.
  Yan Yuanliang, et al. PloS one 2013 0 (10) e78138
• Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women.
  Qin Yingying, et al. Maturitas 2014 1 (1) 64-7
• Association of AQP8 in women with PCOS.
  Li Yang, et al. Reproductive biomedicine online 2013 10 (4) 419-22
• Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome.
  Li Tao, et al. PloS one 2013 0 (7) e66250
• A common polymorphic allele of the LH beta-subunit gene is associated with higher exogenous FSH consumption during controlled ovarian stimulation for assisted reproductive technology.
  Alviggi Carlo, et al. Reproductive biology and endocrinology : RB&E 2013 0 (1) 51
• Mutational analysis of SKP2 and P27 in Chinese Han women with premature ovarian failure.
  Zhao Zhiyi, et al. Reproductive biomedicine online 2013 7 (1) 104-6
• Lack of association of WNT5A mutations with Müllerian duct abnormalities.
  Wu K, et al. Reproductive biomedicine online 2012 10
• Mutations in DMC1 are not responsible for premature ovarian failure in Chinese women.
  Wang H, et al. Reproductive biomedicine online 2012 10
• Association study of gene LPP in women with polycystic ovary syndrome.
  Zhang Bo, et al. PloS one 2012 0 (10) e46370
• The role of male chromosomal polymorphism played in spermatogenesis and the outcome of IVF/ICSI-ET treatment.
  Guo T, et al. International journal of andrology 2012 12 (6) 802-9
• A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.
  Zhao Han, et al. American journal of human genetics 2012 5 (5) 900-6

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Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB