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Premature Ovarian Failure among Fragile X Premutation Carriers: Parent-of-Origin Effect?

American journal of human genetics, 2000-07, Vol.67 (1), p.11-13

Sherman, Stephanie L.

2000

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Association of FMR1 repeat size with ovarian dysfunction

Human reproduction (Oxford), 2005-02, Vol.20 (2), p.402-412

2005

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FMR1 and the fragile X syndrome: Human genome epidemiology review

Genetics in medicine, 2001-09, Vol.3 (5), p.359-371

2001

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Co-occurring diagnoses among FMR1 premutation allele carriers

Clinical genetics, 2010-04, Vol.77 (4), p.374-381

2010

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Association between telomere length and chromosome 21 nondisjunction in the oocyte

Human genetics, 2015-11, Vol.134 (11-12), p.1263-1270

2015

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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

American journal of human genetics, 2003-02, Vol.72 (2), p.454-464

2003

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Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects

Clinical genetics, 2009-02, Vol.75 (2), p.180-184

2009

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Association between Maternal Age and Meiotic Recombination for Trisomy 21

American journal of human genetics, 2005-01, Vol.76 (1), p.91-99

2005

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Effect of meiotic recombination on the production of aneuploid gametes in humans

Cytogenetic and genome research, 2005-01, Vol.111 (3-4), p.250-255

2005

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Polymorphisms in Genes Involved in Folate Metabolism as Maternal Risk Factors for Down Syndrome

American journal of human genetics, 2000-09, Vol.67 (3), p.623-630

2000

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A study of the distributional characteristics of FMR1 transcript levels in 238 individuals

Human genetics, 2004-04, Vol.114 (5), p.439-447

2004

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Association and Linkage of the Dopamine Transporter Gene and Attention-Deficit Hyperactivity Disorder in Children: Heterogeneity owing to Diagnostic Subtype and Severity

American journal of human genetics, 1998-12, Vol.63 (6), p.1767-1776

1998

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Evidence-Based Approach of Treatment Options for Postoperative Knee Pain

The Physician and sportsmedicine, 2014-05, Vol.42 (2), p.58-70

2014

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Risk factors for nondisjunction of trisomy 21

Cytogenetic and genome research, 2005-01, Vol.111 (3-4), p.273-280

2005

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Women with a Reduced Ovarian Complement May Have an Increased Risk for a Child with Down Syndrome

American journal of human genetics, 2000-05, Vol.66 (5), p.1680-1683

2000

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Clinical outcomes of revision biceps tenodesis

International journal of shoulder surgery, 2012-04, Vol.6 (2), p.45-50

2012

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Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size Range

American journal of human genetics, 2002-06, Vol.70 (6), p.1532-1544

2002

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Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21

Human molecular genetics, 1997-09, Vol.6 (9), p.1391-1399

1997

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Familial transmission of the FMR1 CGG repeat

American journal of human genetics, 1996-12, Vol.59 (6), p.1252-1261

1996

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CYP17 genotype predicts serum hormone levels among pre-menopausal women

Human reproduction (Oxford), 2005-08, Vol.20 (8), p.2162-2167

2005

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Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population

American journal of human genetics, 1999-02, Vol.64 (2), p.495-507

1999

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Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status

Genetics in medicine, 2004-11, Vol.6 (6), p.487-494

2004

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The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children

Behavior genetics, 1998-05, Vol.28 (3), p.215-225

1998

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Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans

Human molecular genetics, 1998-08, Vol.7 (8), p.1221-1227

1998

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Risk factors for trisomy 21: maternal cigarette smoking and oral contraceptive use in a population-based case-control study

Genetics in medicine, 1999-03, Vol.1 (3), p.80

1999

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Premature Ovarian Failure among Fragile X Premutation Carriers: Parent-of-Origin Effect?

Association of FMR1 repeat size with ovarian dysfunction

FMR1 and the fragile X syndrome: Human genome epidemiology review

Co-occurring diagnoses among FMR1 premutation allele carriers

Association between telomere length and chromosome 21 nondisjunction in the oocyte

Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects

Association between Maternal Age and Meiotic Recombination for Trisomy 21

Effect of meiotic recombination on the production of aneuploid gametes in humans

Polymorphisms in Genes Involved in Folate Metabolism as Maternal Risk Factors for Down Syndrome

A study of the distributional characteristics of FMR1 transcript levels in 238 individuals

Association and Linkage of the Dopamine Transporter Gene and Attention-Deficit Hyperactivity Disorder in Children: Heterogeneity owing to Diagnostic Subtype and Severity

Evidence-Based Approach of Treatment Options for Postoperative Knee Pain

Risk factors for nondisjunction of trisomy 21

Women with a Reduced Ovarian Complement May Have an Increased Risk for a Child with Down Syndrome

Clinical outcomes of revision biceps tenodesis

Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size Range

Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21

Familial transmission of the FMR1 CGG repeat

CYP17 genotype predicts serum hormone levels among pre-menopausal women

Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population

Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status

The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children

Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans

Risk factors for trisomy 21: maternal cigarette smoking and oral contraceptive use in a population-based case-control study

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