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Localisation of a gene implicated in a severe speech and language disorder

Nature genetics, 1998-02, Vol.18 (2), p.168-170

1998

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Neural Basis of an Inherited Speech and Language Disorder

Proceedings of the National Academy of Sciences - PNAS, 1998-10, Vol.95 (21), p.12695-12700

1998

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

Cell, 1993-07, Vol.74 (1), p.127-134

1993

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IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

Human molecular genetics, 1997-11, Vol.6 (12), p.2179-2185

1997

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Human transgenerational responses to early-life experience: potential impact on development, health and biomedical research

Journal of Medical Genetics, 2014-09, Vol.51 (9), p.563-572

2014

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Factor V Leiden is associated with pre‐eclampsia but not with fetal growth restriction: a genetic association study and meta‐analysis

Journal of thrombosis and haemostasis, 2008-11, Vol.6 (11), p.1868-1875

2008

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Radiological malformations of the ear in pendred syndrome

Clinical radiology, 1998-04, Vol.53 (4), p.268-273

1998

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Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

Science (American Association for the Advancement of Science), 1995-02, Vol.267 (5198), p.685-688

1995

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Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

The Lancet (British edition), 1992-12, Vol.340 (8832), p.1376-1379

1992

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A clinical and genetic study of campomelic dysplasia

Journal of medical genetics, 1995-06, Vol.32 (6), p.415-420

1995

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Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

The Lancet (British edition), 1998-01, Vol.351 (9099), p.311-316

1998

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Transgenerational response to nutrition, early life circumstances and longevity

European journal of human genetics : EJHG, 2007-07, Vol.15 (7), p.784-790

2007

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Uniparental paternal disomy in Angelman's syndrome

The Lancet (British edition), 1991-03, Vol.337 (8743), p.694-697

1991

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Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

Human genetics, 2000-11, Vol.107 (5), p.499-503

2000

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Angelman syndrome

Journal of medical genetics, 1992-06, Vol.29 (6), p.412-415

1992

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Association of the INS VNTR with size at birth

Nature genetics, 1998-05, Vol.19 (1), p.98-100

1998

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ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology

Paediatric and perinatal epidemiology, 2001-01, Vol.15 (1), p.74-87

2001

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The Avon Longitudinal Study of Parents and Children (ALSPAC): a resource for genetic epidemiology

European journal of endocrinology, 2004-11, Vol.151 Suppl 3 (Suppl_3), p.U125-U129

Pembrey, Marcus

2004

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An assessment of screening strategies for fragile X syndrome in the UK

Health technology assessment (Winchester, England), 2001, Vol.5 (7), p.1-95

2001

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The association of aneuploidy and mild fetal pyelectasis in an unselected population: the results of a multicenter study

Ultrasound in obstetrics & gynecology, 2001-03, Vol.17 (3), p.197-202

2001

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Hyperphagic short stature and Prader–Willi syndrome: A comparison of behavioural phenotypes, genotypes and indices of stress

British journal of psychiatry, 2001-08, Vol.179 (2), p.129-137

2001

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Sex-specific, male-line transgenerational responses in humans

European journal of human genetics : EJHG, 2006-02, Vol.14 (2), p.159-166

2006

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Imprinting and transgenerational modulation of gene expression; human growth as a model

Acta geneticae medicae et gemellologiae, 1996, Vol.45 (1-2), p.111-125

Pembrey, M

1996

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Sex-specific, male-line transgenerational responses in humans

European journal of human genetics : EJHG, 2006-02, Vol.14 (2), p.159-166

2006

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Rheumatoid arthritis association at 6q23

Nature genetics, 2007-12, Vol.39 (12), p.1431-1433

2007

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Localisation of a gene implicated in a severe speech and language disorder

Neural Basis of an Inherited Speech and Language Disorder

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

Human transgenerational responses to early-life experience: potential impact on development, health and biomedical research

Factor V Leiden is associated with pre‐eclampsia but not with fetal growth restriction: a genetic association study and meta‐analysis

Radiological malformations of the ear in pendred syndrome

Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

A clinical and genetic study of campomelic dysplasia

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

Transgenerational response to nutrition, early life circumstances and longevity

Uniparental paternal disomy in Angelman's syndrome

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

Angelman syndrome

Association of the INS VNTR with size at birth

ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology

The Avon Longitudinal Study of Parents and Children (ALSPAC): a resource for genetic epidemiology

An assessment of screening strategies for fragile X syndrome in the UK

The association of aneuploidy and mild fetal pyelectasis in an unselected population: the results of a multicenter study

Hyperphagic short stature and Prader–Willi syndrome: A comparison of behavioural phenotypes, genotypes and indices of stress

Sex-specific, male-line transgenerational responses in humans

Imprinting and transgenerational modulation of gene expression; human growth as a model

Sex-specific, male-line transgenerational responses in humans

Rheumatoid arthritis association at 6q23

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