Genetics of primary ovarian insufficiency: New developments and opportunities

Human Reproduction Update

Volumn 21, Issue 6, 2015, Pages 787-808

  Qin, Yingying ^a   Jiao, Xue ^a   Simpson, Joe Leigh ^b,c   Chen, Zi Jiang ^a,d  

^a SHANDONG UNIVERSITY   (China)

^b March of Dimes Birth Defects Foundation   (United States)

^c FLORIDA INTERNATIONAL UNIVERSITY   (United States)

^d SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

Chromosomal abnormality; Gene mutation; Genome wide association studies; Next generation sequencing; Premature ovarian failure; Primary ovarian insufficiency; Whole exome sequencing

Indexed keywords

ANDROGEN RECEPTOR; BONE MORPHOGENETIC PROTEIN 15; FOLLITROPIN RECEPTOR; FRAGILE X MENTAL RETARDATION PROTEIN; GROWTH DIFFERENTIATION FACTOR 9; MINICHROMOSOME MAINTENANCE PROTEIN 8; MINICHROMOSOME MAINTENANCE PROTEIN 9; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 3; WNT4 PROTEIN;

ANDROGEN RECEPTOR GENE; ARTICLE; ATP DEPENDENT DNA HELICASE HOMOLOG GENE; BONE MORPHOGENETIC PROTEIN 15 GENE; CHROMOSOME ABERRATION; CHROMOSOME DELETION X; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION X; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DACHSHUND FAMILY TRANSCRIPTION FACTOR 2 GENE; FOLLICULOGENESIS SPECIFIC BHLH TRANSCRIPTION FACTOR GENE; FORKHEAD BOX O4 GENE; FRAGILE X MENTAL RETARDATION I GENE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETICS; GROWTH DIFFERENTIATION FACTOR 9 GENE; HUMAN; ISOCHROMOSOME; KARYOTYPING; LINKAGE ANALYSIS; MINICHROMOSOME MAINTENANCE COMPLEX COMPONENT 8 GENE; MINICHROMOSOME MAINTENANCE COMPLEX COMPONENT 9 GENE; MITOCHONDRIAL GENE; MONOSOMY X; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; NANOS HOMOLOG 3 GENE; NEWBORN OVARY HOMEOBOX GENE; NUCLEAR RECEPTOR SUBFAMILY 5 GROUP A MEMBER I GENE; PREMATURE OVARIAN FAILURE; PREMATURE OVARIAN FAILURE 1B GENE; PRIORITY JOURNAL; PROGESTERONE RECEPTOR MEMBRANE COMPONENT I GENE; REGULATOR GENE; STROMAL ANTIGEN 3 GENE; SYNAPTONEMAL COMPLEX CENTRAL ELEMENT 1 GENE; TURNER SYNDROME; EXOME; FEMALE; GENE REGULATORY NETWORK; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOMICS;

CHROMOSOME ABERRATIONS; EXOME; FEMALE; GENE REGULATORY NETWORKS; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HUMANS; KARYOTYPING; MOSAICISM; PRIMARY OVARIAN INSUFFICIENCY;

EID: 84947562583     PISSN: 13554786     EISSN: 14602369     Source Type: Journal    
DOI: 10.1093/humupd/dmv036     Document Type: Article

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