AHEC Digital Library - Genetics

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"Genetics" (56 records)

Altered Levels of Mitochondrial DNA Are Associated with Female Age, Aneuploidy, and Provide an Independent Measure of Embryonic Implantation Potential
No Pub/Vend Assigned
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.
No Pub/Vend Assigned
Cell-free DNA in Human Follicular Microenvironment: New Prognostic Biomarker to Predict in vitro Fertilization Outcomes
No Pub/Vend Assigned
Cell-free DNA testing for 22q11.2 deletion syndrome: appraising the viability, effectiveness and appropriateness of screening
Wiley
Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities
No Pub/Vend Assigned
Clinical management of mosaic results from preimplantation genetic testing for aneuploidy (PGT-A) of blastocysts: a committee opinion
No Pub/Vend Assigned
Clinical Trials at Duke
Medical Center
Clinical Trials at WFU
Baptist Medical Center
Clinical, hormonal, ovarian, and genetic aspects of 46,XX patients with congenital adrenal hyperplasia due to CYP17A1 defects.
Elsevier
ClinicalTrials.gov
ClinicalTrials.gov
Detecting mosaicism in trophectoderm biopsies: current challenges and future possibilities.
Oxford University Press
Diagnosis and clinical management of embryonic mosaicism.
No Pub/Vend Assigned
Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial.
JAMA Network
Effect of oophorectomy on survival after breast cancer in BRCA1 and BRCA2 mutation carriers.
No Pub/Vend Assigned
Effect of Timing by Endometrial Receptivity Testing vs Standard Timing of Frozen Embryo Transfer on Live Birth in Patients Undergoing In Vitro Fertilization
JAMA Network
Euploidy rates between cycles triggered with gonadotropin-releasing hormone agonist and human chorionic gonadotropin
No Pub/Vend Assigned
GenBank: NIH database of publicly available DNA sequences
National Center for Biotechnology Information
GeneReviews
University of Washington
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
No Pub/Vend Assigned
Genetic Testing Registry (GTR)
University of Washington
Genetics Home Reference
National Center for Biotechnology Information
Genome Biology
BioMed Central
Genome Database
National Center for Biotechnology Information
Genome Medicine
BioMed Central
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
Nature
Hormone Replacement Therapy After Oophorectomy and Breast Cancer Risk Among BRCA1 Mutation Carriers.
JAMA
Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients
National Library of Medicine (NLM)
Integrated genomic and molecular characterization of cervical cancer.
Nature
Live Birth with or without Preimplantation Genetic Testing for Aneuploidy
New England Journal of Medicine
Live births following karyomapping of human blastocysts: Experience from clinical application of the method.
American Board of Obstetrics and Gynecology
MedlinePlus
MedlinePlus
MedlinePlus - Genetics/Birth Defects Topics
MedlinePlus
The methylenetetrahydrofolate reductase c.c.677 C>T and c.c.1298 A>C polymorphisms in reproductive failures: Experience from an RSA and RIF study on a Polish population.
PLoS
Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks
No Pub/Vend Assigned
Mutations in homologous recombination genes and outcomes in ovarian carcinoma patients in GOG 218: an NRG oncology/gynecologic oncology group study.
No Pub/Vend Assigned
National estimates of genetic testing in women with a history of breast or ovarian cancer.
ABOG
NC TraCS Institute
UNC Chapel Hill
Olaparib Versus Nonplatinum Chemotherapy in Patients With Platinum-Sensitive Relapsed Ovarian Cancer and a Germline BRCA1/2 Mutation (SOLO3): A Randomized Phase III Trial
ASCO
OMIM (authoritative compendium of human genes and genetic phenotypes)
National Center for Biotechnology Information
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study
Elsevier
Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA
Elsevier
Practical guidelines for managing adults with 22q11.2 deletion syndrome
No Pub/Vend Assigned
Prediction model for aneuploidy in early human embryo development revealed by single-cell analysis.
No Pub/Vend Assigned
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial
PubMed
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
No Pub/Vend Assigned
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
No Pub/Vend Assigned
PubMed MEDLINE
PubMed
RCA reversion mutations in circulating tumor DNA predict primary and acquired resistance to the PARP inhibitor rucaparib in high-grade ovarian carcinoma.
No Pub/Vend Assigned
Research & Innovation at UNC (look here for Clinical Trials info)
UNC Healthcare
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings
American Journal of Obstetrics and Gynecology
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
JAMA Network
Risk of fetal loss associated with invasive testing following combined first-trimester screening for Down syndrome: a national cohort of 147 987 singleton pregnancies
No Pub/Vend Assigned
Special Report of the Society for Maternal-Fetal Medicine Placenta Accreta Spectrum Ultrasound Marker Task Force: Consensus on definition of markers and approach to the ultrasound examination in pregnancies at risk for placenta accreta spectrum
Elsevier
Structure Databases
National Center for Biotechnology Information
Taxonomy Resources
National Center for Biotechnology Information
Using outcome data from one thousand mosaic embryo transfers to formulate an embryo ranking system for clinical use
No Pub/Vend Assigned

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