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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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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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Co-occurring diagnoses among FMR1 premutation allele carriers

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

2010

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Examination of reproductive aging milestones among women who carry the FMR1 premutation

Human reproduction (Oxford), 2007-08, Vol.22 (8), p.2142-2152

2007

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Germline mutation of microRNA-125a is associated with breast cancer

Journal of medical genetics, 2009-05, Vol.46 (5), p.358-360

2009

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Animal models of cartilage repair

Bone & joint research, 2014-04, Vol.3 (4), p.89-94

2014

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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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Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study

Human reproduction (Oxford), 2008-05, Vol.23 (5), p.1220-1225

2008

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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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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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Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery

Journal of medical genetics, 2008-05, Vol.45 (5), p.290-297

2008

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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 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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Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency

Human reproduction (Oxford), 2016-01, Vol.31 (1), p.158-168

2016

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Mercury isotopic composition of hydrothermal systems in the Yellowstone Plateau volcanic field and Guaymas Basin sea-floor rift

Earth and planetary science letters, 2009-03, Vol.279 (1), p.86-96

2009

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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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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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Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II

Nature genetics, 1996-12, Vol.14 (4), p.400-405

1996

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Renal masses: assessment of corticomedullary-phase and nephrographic-phase CT scans

Radiology, 1995-08, Vol.196 (2), p.445

1995

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Hyaluronan accumulates in demyelinated lesions and inhibits oligodendrocyte progenitor maturation

Nature medicine, 2005-09, Vol.11 (9), p.966-972

2005

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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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Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error : A population-based study

American journal of human genetics, 1996-03, Vol.58 (3), p.628-633

1996

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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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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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Ruffling membrane, stress fiber, cell spreading and proliferation abnormalities in human Schwannoma cells

Oncogene, 1998-10, Vol.17 (17), p.2195-2209

1998

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