Grant W Montgomery

No ORCID on file · 206 papers in corpus · active 2002-2026

Study types

  • article 115
  • other 24
  • review 23
  • preprint 10
  • meta-analysis 4

Condition tags

  • endometriosis 180
  • infertility 22
  • chronic_pelvic_pain 7
  • adenomyosis 5
  • dysmenorrhea 4
  • irritable_bowel_syndrome 3
  • die_deep_infiltrating 2
  • endometrioma 1
review 2015
Twin research and human genetics : the official journal of the International Society for Twin Studies ·doi:10.1017/thg.2015.61

Endometriosis is a complex disease that affects 6-10% of women in their reproductive years and 20-50% of women with infertility. Genome-wide and candidate-gene association studies for endometriosis have identified 10 independent risk loci, …

article 2015

Abstract: Endometriosis is a complex disease involving multiple susceptibility genes and environmental factors. Our pre-vious studies on endometriosis identified a region of significant linkage on chromosome 10q. Two biological candidate ge…

article 2015
Human molecular genetics ·doi:10.1093/hmg/ddv306

Epidemiological studies have demonstrated associations between endometriosis and certain histotypes of ovarian cancer, including clear cell, low-grade serous and endometrioid carcinomas. We aimed to determine whether the observed associatio…

article 2015

Epidemiological studies have demonstrated associations between endometriosis and certain histotypes of ovarian cancer, including clear cell, low-grade serous and endometrioid carcinomas. We aimed to determine whether the observed associatio…

review 2014
Human Reproduction ·doi:10.1093/humrep/deu267

STUDY QUESTION: Are single-nucleotide polymorphisms (SNPs) at the interleukin 1A (IL1A) gene locus associated with endometriosis risk? SUMMARY ANSWER: We found evidence for strong association between IL1A SNPs and endometriosis risk. WHAT I…

article 2014
Fertility and sterility ·doi:10.1016/j.fertnstert.2014.04.015

ObjectiveTo follow-up previous studies highlighting a possible role for cytochrome P450, family 2, subfamily C, 19 (CYP2C19) in susceptibility to endometriosis by searching for additional variants in the CYP2C19 gene that may be associated …

2014
Nature genetics ·doi:10.1038/ng.3079

Primary open-angle glaucoma (POAG) is a major cause of irreversible blindness worldwide. We performed a genome-wide association study in an Australian discovery cohort comprising 1,155 cases with advanced POAG and 1,992 controls. We investi…

review 2014
Human reproduction update ·doi:10.1093/humupd/dmu015

BACKGROUND: Endometriosis is a heritable common gynaecological condition influenced by multiple genetic and environmental factors. Genome-wide association studies (GWASs) have proved successful in identifying common genetic variants of mode…

article 2014

BACKGROUND Endometriosis is a heritable common gynaecological condition influenced by multiple genetic and environmental factors. Genome-wide association studies (GWASs) have proved successful in identifying common genetic variants of moder…

article 2014
2014
Journal of the National Cancer Institute ·doi:10.1093/jnci/dju267

Telomere length has been associated with risk of many cancers, but results are inconsistent. Seven single nucleotide polymorphisms (SNPs) previously associated with mean leukocyte telomere length were either genotyped or well-imputed in 111…

article 2014
Fertility and sterility ·doi:10.1016/j.fertnstert.2014.07.1209

OBJECTIVE: To harmonize standard operating procedures (SOPs) and standardize the recording of associated data for collection, processing, and storage of human tissues relevant to endometriosis. DESIGN: An international collaboration involvi…

review 2014
Fertility and sterility ·doi:10.1016/j.fertnstert.2014.07.1244

OBJECTIVE: To harmonize the collection of nonsurgical clinical and epidemiologic data relevant to endometriosis research, allowing large-scale collaboration. DESIGN: An international collaboration involving 34 clinical/academic centers and …

review 2014
Fertility and sterility ·doi:10.1016/j.fertnstert.2014.07.1208

OBJECTIVE: To harmonize standard operating procedures (SOPs) and standardize the recording of associated data for collection, processing, and storage of fluid biospecimens relevant to endometriosis. DESIGN: An international collaboration in…

article 2013
·doi:10.1158/1538-7445.am2013-3182

Abstract While endometriosis is a known risk factor for endometrioid and clear-cell ovarian cancer subtypes, a convincing link between endometriosis and endometrial cancer has been difficult to establish epidemiologically. Such a link has b…

2013
Carcinogenesis ·doi:10.1093/carcin/bgs407

Genome-wide association studies (GWASs) have mainly focused on top significant single nucleotide polymorphisms (SNPs), most of which did not have clear biological functions but were just surrogates for unknown causal variants. Studying SNPs…

2013
Pigment cell & melanoma research ·doi:10.1111/pcmr.12069

To mine possibly hidden causal single-nucleotide polymorphisms (SNPs) of melanoma, we investigated the association of SNPs in 76 M/G1 transition genes with melanoma risk using our published genome-wide association study (GWAS) data set with…

article 2013
Reproductive sciences (Thousand Oaks, Calif.) ·doi:10.1177/1933719113477495

Endometriosis, defined as estrogen-dependent lesions containing endometrial glands and stroma outside the uterus, is a chronic and often painful gynecological condition that affects 6% to 10% of reproductive age women. Endometriosis has est…

other 2013
Human molecular genetics ·doi:10.1093/hmg/dds491

Common diseases such as endometriosis (ED), Alzheimer's disease (AD) and multiple sclerosis (MS) account for a significant proportion of the health care burden in many countries. Genome-wide association studies (GWASs) for these diseases ha…

article 2013

Genome-wide association studies show strong evidence of association with endometriosis for markers on chromosome 1p36 spanning the potential candidate genes WNT4, CDC42 and LINC00339. WNT4 is involved in development of the uterus, and the e…

article 2013
International journal of molecular epidemiology and genetics

Genome-wide association studies show strong evidence of association with endometriosis for markers on chromosome 1p36 spanning the potential candidate genes WNT4, CDC42 and LINC00339. WNT4 is involved in development of the uterus, and the e…

2013
Nature genetics ·doi:10.1038/ng.2711

Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across disorders is unclear. To examine shared genetic etiology, we use genome-wide genotype da…

article 2013
article 2013
article 2013
·doi:10.1093/humrep/det161