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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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Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms

American journal of human genetics, 2005-05, Vol.76 (5), p.773-779

2005

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Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

American journal of human genetics, 2012-04, Vol.90 (4), p.715-719

2012

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A Common Haplotype of the Glucokinase Gene Alters Fasting Glucose and Birth Weight: Association in Six Studies and Population-Genetics Analyses

American journal of human genetics, 2006-12, Vol.79 (6), p.991-1001

2006

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Male-line transgenerational responses in humans

Human fertility (Cambridge, England), 2010-12, Vol.13 (4), p.268-271

Pembrey, Marcus E.

2010

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Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals

American journal of human genetics, 2007-06, Vol.80 (6), p.1150-1161

2007

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β2-adrenoceptor polymorphisms and asthma from childhood to middle age in the British 1958 birth cohort: a genetic association study

The Lancet (British edition), 2006-08, Vol.368 (9537), p.771-779

2006

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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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Epigenomic socioeconomic studies more similar than different

Proceedings of the National Academy of Sciences - PNAS, 2013-04, Vol.110 (14), p.E1246-E1246

2013

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Does cross-generational epigenetic inheritance contribute to cultural continuity?

Environmental epigenetics, 2018-04, Vol.4 (2), p.dvy004-dvy004

Pembrey, Marcus E

2018

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Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1128-1133

2004

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Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population

The American journal of psychiatry, 2008-12, Vol.165 (12), p.1576-1584

2008

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Paternal grandmother’s smoking in pregnancy is associated with extreme aversion to bitter taste in their grandchildren

Environmental epigenetics, 2022, Vol.8 (1), p.dvac003-dvac003

2022

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Time to take epigenetic inheritance seriously

European journal of human genetics : EJHG, 2002-11, Vol.10 (11), p.669-671

Pembrey, Marcus E

2002

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Unexpected Associations between the Number of FRAXE Repeats in Boys and Evidence of Diabetes in Their Mothers and Maternal Grandmothers

OBM Genetics, 2021-10, Vol.5 (4), p.15-1

2021

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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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Change in paternal grandmothers' early food supply influenced cardiovascular mortality of the female grandchildren

BMC genetics, 2014, Vol.15, p.12

2014

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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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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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Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans

BMC genetics, 2005-05, Vol.6, p.22

2005

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Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS

American journal of medical genetics, 2004-03, Vol.125A (2), p.167-172

2004

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Behavioural, psychiatric, and cognitive phenotypes associated with numbers of repeats of the FRAXE allele on the FMR2 gene

Wellcome open research, 2024, Vol.9, p.238

2024

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Genetic variation in the type 2 insulin-like growth factor receptor gene and disparity in childhood height

Growth hormone & IGF research, 2005-12, Vol.15 (6), p.363-368

2005

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Sex-specific, male-line transgenerational responses in humans (Reprinted from EUROPEAN JOURNAL OF HUMAN GENETICS, vol 14 pg 159-166, 2006)

European journal of human genetics : EJHG, 2017-05, Vol.25, p.S95

2017

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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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Sex-specific, male-line transgenerational responses in humans

Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms

Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

A Common Haplotype of the Glucokinase Gene Alters Fasting Glucose and Birth Weight: Association in Six Studies and Population-Genetics Analyses

Male-line transgenerational responses in humans

Type 2 Diabetes TCF7L2 Risk Genotypes Alter Birth Weight: A Study of 24,053 Individuals

β2-adrenoceptor polymorphisms and asthma from childhood to middle age in the British 1958 birth cohort: a genetic association study

Sex-specific, male-line transgenerational responses in humans

Epigenomic socioeconomic studies more similar than different

Does cross-generational epigenetic inheritance contribute to cultural continuity?

Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population

Paternal grandmother’s smoking in pregnancy is associated with extreme aversion to bitter taste in their grandchildren

Time to take epigenetic inheritance seriously

Unexpected Associations between the Number of FRAXE Repeats in Boys and Evidence of Diabetes in Their Mothers and Maternal Grandmothers

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

Change in paternal grandmothers' early food supply influenced cardiovascular mortality of the female grandchildren

Association of the INS VNTR with size at birth

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

Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans

Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS

Behavioural, psychiatric, and cognitive phenotypes associated with numbers of repeats of the FRAXE allele on the FMR2 gene

Genetic variation in the type 2 insulin-like growth factor receptor gene and disparity in childhood height

Sex-specific, male-line transgenerational responses in humans (Reprinted from EUROPEAN JOURNAL OF HUMAN GENETICS, vol 14 pg 159-166, 2006)

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

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