Precision reproductive medicine: multigene panel testing for infertility risk assessment
出版年份 2017 全文链接
标题
Precision reproductive medicine: multigene panel testing for infertility risk assessment
作者
关键词
Precision medicine, Reproductive genetics, Multigene panel testing, Genetic predisposition to disease, Infertility
出版物
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
Volume 34, Issue 8, Pages 967-973
出版商
Springer Nature
发表日期
2017-05-03
DOI
10.1007/s10815-017-0938-y
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Adding Protective Genetic Variants to Clinical Reporting of Genomic Screening Results
- (2017) Marci L. B. Schwartz et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1
- (2017) A H Smith et al. MOLECULAR PSYCHIATRY
- Routine use of gene panel testing in hereditary breast cancer should be performed with caution
- (2016) Cedric van Marcke et al. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
- Improving performance of multigene panels for genomic analysis of cancer predisposition
- (2016) Brian H. Shirts et al. GENETICS IN MEDICINE
- Pharmacogenetics: The right drug for you
- (2016) Liam Drew NATURE
- The genetics of drug efficacy: opportunities and challenges
- (2016) Matthew R. Nelson et al. NATURE REVIEWS GENETICS
- Developing and evaluating polygenic risk prediction models for stratified disease prevention
- (2016) Nilanjan Chatterjee et al. NATURE REVIEWS GENETICS
- The Role of Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer
- (2016) Lynn C. Hartmann et al. NEW ENGLAND JOURNAL OF MEDICINE
- Precision Medicine in Assisted Conception: A Multicenter Observational Treatment Cohort Study of the Annexin A5 M2 Haplotype as a Biomarker for Antithrombotic Treatment to Improve Pregnancy Outcome
- (2016) Simon Fishel et al. EBioMedicine
- Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients
- (2016) Kentaro Mori et al. PLoS One
- Understanding of BRCA VUS genetic results by breast cancer specialists
- (2015) B. K. Eccles et al. BMC CANCER
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening
- (2015) Melissa K. Frey et al. GYNECOLOGIC ONCOLOGY
- Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials
- (2015) Jessica L Mega et al. LANCET
- Protective alleles and modifier variants in human health and disease
- (2015) Andrew R. Harper et al. NATURE REVIEWS GENETICS
- The FDA and Genomic Tests — Getting Regulation Right
- (2015) Barbara J. Evans et al. NEW ENGLAND JOURNAL OF MEDICINE
- Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk
- (2015) Douglas F. Easton et al. NEW ENGLAND JOURNAL OF MEDICINE
- A New Initiative on Precision Medicine
- (2015) Francis S. Collins et al. NEW ENGLAND JOURNAL OF MEDICINE
- Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory
- (2014) D. Cragun et al. CLINICAL GENETICS
- Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes
- (2014) Laurent Castéra et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients
- (2014) Holly LaDuca et al. GENETICS IN MEDICINE
- Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment
- (2014) Allison W. Kurian et al. JOURNAL OF CLINICAL ONCOLOGY
- Cost-effectiveness of Population Screening for BRCA Mutations in Ashkenazi Jewish Women Compared With Family History–Based Testing
- (2014) Ranjit Manchanda et al. JNCI-Journal of the National Cancer Institute
- Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
- (2014) Jae Yeon Cheon et al. Genome Medicine
- The FMR1 gene, infertility, and reproductive decision-making: a review
- (2014) Lisa M. Pastore et al. Frontiers in Genetics
- Genetic Testing in the Diagnosis of Primary Ciliary Dyskinesia: State-of-the-Art and Future Perspectives
- (2014) Samuel Collins et al. Journal of Clinical Medicine
- Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes
- (2013) Michael O. Dorschner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Adult Genetic Risk Screening
- (2013) C. Thomas Caskey et al. Annual Review of Medicine
- StuI polymorphism on the androgen receptor gene is associated with recurrent spontaneous abortion
- (2013) Tahere Jahaninejad et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Personalized reproductive medicine on the brink: progress, opportunities and challenges ahead
- (2013) Piraye Yurttas Beim et al. REPRODUCTIVE BIOMEDICINE ONLINE
- Day 3 embryo selection by metabolomic profiling of culture medium with near-infrared spectroscopy as an adjunct to morphology: a randomized controlled trial
- (2012) C. G. Vergouw et al. HUMAN REPRODUCTION
- Impact of follicle stimulating hormone receptor variants in fertility
- (2011) Maria D Lalioti CURRENT OPINION IN OBSTETRICS & GYNECOLOGY
- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
- (2011) M. J. Ackerman et al. EUROPACE
- Essential Elements of Genetic Cancer Risk Assessment, Counseling, and Testing: Updated Recommendations of the National Society of Genetic Counselors
- (2011) Bronson D. Riley et al. Journal of Genetic Counseling
- Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers With Cancer Risk and Mortality
- (2010) Susan M. Domchek JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Health Behavior Changes After Genetic Risk Assessment for Alzheimer Disease: The REVEAL Study
- (2009) Serena Chao et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Distress among women receiving uninformativeBRCA1/2results: 12-month outcomes
- (2009) Suzanne C. O'Neill et al. PSYCHO-ONCOLOGY
- Genome-based prediction of common diseases: advances and prospects
- (2008) A. C. J.W. Janssens et al. HUMAN MOLECULAR GENETICS
- Currents in Contemporary Ethics GINA, the ADA, and Genetic Discrimination in Employment
- (2008) Mark A. Rothstein JOURNAL OF LAW MEDICINE & ETHICS
- Ovulatory Response to Treatment of Polycystic Ovary Syndrome Is Associated with a Polymorphism in theSTK11Gene
- (2007) Richard S. Legro et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now