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1

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

Fisher, Simon E., Vargha-Khadem, Faraneh, Watkins, Kate E., Monaco, Anthony P., Pembrey, Marcus E.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 365 KB

1998

2

Transgenerational epigenetic inheritance: how important is it?

Grossniklaus, Ueli, Kelly, Bill, Ferguson-Smith, Anne C., Pembrey, Marcus, Lindquist, Susan

Journal:

Nature Reviews Genetics

Year:

2013

Language:

english

File:

PDF, 205 KB

english, 2013

3

Sex-specific, male-line transgenerational responses in humans

Pembrey, Marcus E, Bygren, Lars Olov, Kaati, Gunnar, Edvinsson, Sören, Northstone, Kate, Sjöström, Michael, Golding, Jean

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 112 KB

english, 2005

4

Prevalence of Mitochondrial 1555A→G Mutation in European Children

Bitner-Glindzicz, Maria, Pembrey, Marcus, Duncan, Andrew, Heron, Jon, Ring, Susan M., Hall, Amanda, Rahman, Shamima

Journal:

Boston Medical and Surgical Journal

Year:

2009

Language:

english

File:

PDF, 198 KB

english, 2009

5

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?

Sylvain Briault, Laurent Villard, Ute Rogner, Johannes Coy, Sylvie Odent, Josette Lucas, Edith Passage, Danping Zhu, Antony Shrimpton, Marcus Pembrey, Marianne Till, Agnès Guichet, Sabine Dessay, Mich

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 1.85 MB

english, 2000

6

FG syndrome: Linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]

Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, John M. Opitz, Helen Middleton-Price, Marcus Pembrey, Claude Moraine, Sylvain Briault

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 211 KB

english, 2002

7

In Memoriam: Professor C. O. Carter, MA, DM Oxon, FRCP

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 188 KB

english, 1984

8

Concordance and recessive inheritance of Leber congenital amaurosis

Scott R. Lambert, Stephanie Sherman, David Taylor, Anthony Kriss, Rebecca Coffey, Marcus Pembrey

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 271 KB

english, 1993

9

Difference in methylation patterns within the D15S9 region of chromosome 15qll–13 in first cousins with Angelman syndrome and Prader–Willi syndrome

Dr. Jill Clayton-Smith, Daniel J. Driscoll, Michael F. Waters, Tessa Webb, Tony Andrews, Sue Malcolm, Marcus E. Pembrey, Robert D. Nicholls

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 378 KB

english, 1993

10

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis

Li Ni, Michael J. Wagner, William J. Kimberling, Marcus E. Pembrey, Kenneth M. Grundfast, Shrawan Kumar, Stephen P. Daiger, Dan E. Wells, Kristin Johnson, Richard J. H. Smith

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 522 KB

english, 1994

11

Phenotypic manifestations of branchiootorenal syndrome

Achih Chen, Mary Francis, Li Ni, Cor W. R. J. Cremers, William J. Kimberling, Yutaka Sato, Peter D. Phelps, Susan C. Bellman, Michael J. Wagner, Marcus Pembrey, Richard J. H. Smith

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 659 KB

english, 1995

12

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

Megan P. Hitchins, Sarah Rickard, Fatima Dhalla, Bert B.A. de Vries, Robin Winter, Marcus E. Pembrey, Sue Malcolm

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 80 KB

english, 2004

13

Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS (Am J Med Genet 125A: 167–172)

Megan P. Hitchins, Sarah Rickard, Fatima Dhalla, Bert B.A. de Vries, Robin Winter, Marcus E. Pembrey, Sue Malcolm

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 27 KB

english, 2005

14

Common polymorphism inH19associated with birthweight and cord blood IGF-II levels in humans

Clive J Petry, Ken K Ong, Bryan J Barratt, Diane Wingate, Heather J Cordell, Susan M Ring, Marcus E Pembrey, The ALSPAC Study Team, Wolf Reik, John A Todd, David B Dunger

Journal:

Year:

2005

Language:

english

File:

PDF, 1005 KB

english, 2005

15

Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus

Robin Winter, Marcus Pembrey

Journal:

Year:

1987

Language:

english

File:

PDF, 232 KB

english, 1987

16

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

Jessica Tyson, Lisbeth Tranebjærg, Meriel McEntagart, Lars Larsen, Michael Christiansen, Margo Whiteford, Jørn Bathen, Bjørn Aslaksen, Svein Sørland, Ole Lund, Marcus Pembrey, Sue Malcolm, Maria Bitne

Journal:

Year:

2001

Language:

english

File:

PDF, 13 KB

english, 2001

17

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

Jessica Tyson, Lisbeth Tranebjærg, Meriel McEntagart, Lars Larsen, Michael Christiansen, Margo Whiteford, Jørn Bathen, Bjørn Aslaksen, Svein Sørland, Ole Lund, Marcus Pembrey, Sue Malcolm, Maria Bitne

Journal:

Year:

2000

Language:

english

File:

PDF, 64 KB

english, 2000

18

The search for genenotype/phenotype associations and the phenome scan

Richard Jones, Marcus Pembrey, Jean Golding, David Herrick

Journal:

Paediatric and Perinatal Epidemiology

Year:

2005

Language:

english

File:

PDF, 200 KB

english, 2005

19

Human inheritance, differences and diseases: putting genes in their place. Part I

Journal:

Paediatric and Perinatal Epidemiology

Year:

2008

Language:

english

File:

PDF, 351 KB

english, 2008

20

Human inheritance, differences and diseases: putting genes in their place. Part II

Journal:

Paediatric and Perinatal Epidemiology

Year:

2008

Language:

english

File:

PDF, 189 KB

english, 2008

21

Do we need gene therapy?

PEMBREY, MARCUS E.

Journal:

Year:

1984

File:

PDF, 149 KB

1984

22

Raising the tone of DNA sequences

PEMBREY, MARCUS, HART, DAVID

Journal:

Year:

1984

File:

PDF, 137 KB

1984

23

Genetic prediction of cystic fibrosis

PEMBREY, MARCUS E., MALCOLM, SUE

Journal:

Year:

1986

File:

PDF, 134 KB

1986

24

Germ-line quandary

PEMBREY, MARCUS

Journal:

Year:

1988

File:

PDF, 135 KB

1988

25

Cohort of genes

PEMBREY, MARCUS E.

Journal:

Year:

1990

File:

PDF, 131 KB

1990

26

Isodisomy in BWS chromosomes

WILKIE, ANDREW O. M., MALCOLM, SUSAN, PEMBREY, MARCUS E.

Journal:

Year:

1991

File:

PDF, 147 KB

1991

27

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

Britton, Keith, Pembrey, Marcus, Reardon, William, Trembath, Richard, Coyle, Beth, Coffey, Rebecca, Armour, John A.L., Gausden, Eleanor, Hochberg, Ze'ev, Grossman, Ashley

Journal:

Nature Genetics

Year:

1996

File:

PDF, 314 KB

1996

28

Association of the INS VNTR with size at birth

Dunger, David B., Ong, Ken K.L., Huxtable, Stewart J., Sherriff, Andrea, Woods, Kathryn A., Ahmed, Marion L., Golding, Jean, Pembrey, Marcus E., Ring, Sue, Bennett, Simon T.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 374 KB

1998

29

In the light of preimplantation genetic diagnosis: some ethical issues in medical genetics revisited

Pembrey, Marcus E

Journal:

European Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 90 KB

english, 1998

30

Chinese amend policy on sterilisation for genetic reasons

Pembrey, Marcus, Aymé, Ségolène

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 14 KB

english, 1999

31

A new human genetic resource: a DNA bank established as part of the Avon Longitudinal Study of Pregnancy and Childhood (ALSPAC)

Jones, Richard W, Ring, Susan, Tyfield, Linda, Hamvas, Renata, Simmons, Hugh, Pembrey, Marcus, Golding, Jean, Team, ALSPAC Study

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 168 KB

english, 2000

32

Time to take epigenetic inheritance seriously

Pembrey, Marcus E

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 54 KB

english, 2002

33

Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome

Raynaud, Martine, Dessay, Sabine, Ronce, Nathalie, Opitz, John, Pembrey, Marcus, Romano, Corrado, Moraine, Claude, Briault, Sylvain

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 91 KB

english, 2003

34

Genetic information and testing in insurance and employment: technical, social and ethical issues

Godard, Béatrice, Raeburn, Sandy, Pembrey, Marcus, Bobrow, Martin, Farndon, Peter, Aymé, Ségolène

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 200 KB

english, 2003

35

Reply to Senn

Bygren, Lars Olov, Kaati, Gunnar, Edvinsson, Sören, Pembrey, Marcus E

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 48 KB

english, 2006

36

Transgenerational response to nutrition, early life circumstances and longevity

Kaati, Gunnar, Bygren, Lars Olov, Pembrey, Marcus, Sjöström, Michael

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 111 KB

english, 2007

37

Genetic epidemiology: some special contributions of birth cohorts

Journal:

Paediatric and Perinatal Epidemiology

Year:

2004

Language:

english

File:

PDF, 63 KB

english, 2004

38

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

Miho Ishida, David Monk, Andrew J. Duncan, Sayeda Abu-Amero, Jiehan Chong, Susan M. Ring, Marcus E. Pembrey, Peter C. Hindmarsh, John C. Whittaker, Philip Stanier, Gudrun E. Moore

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 293 KB

english, 2012

39

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome

Eleanor Gausden, John A. L. Armour, Beth Coyle, Rebecca Coffey, Ze'ev Hochberg, Marcus Pembrey, Keith E. Britton, Ashley Grossman, William Reardon, Richard Trembath

Journal:

Clinical Endocrinology

Year:

1996

Language:

english

File:

PDF, 127 KB

english, 1996

40

Jean Golding and Paediatric and Perinatal Epidemiology: Practising What She Preaches

Journal:

Paediatric and Perinatal Epidemiology

Year:

2012

Language:

english

File:

PDF, 69 KB

english, 2012

41

Mapping and cloning hereditary deafness genes

Frans PM Cremers, Maria Bitner-Glindzicz, Marcus E Pembrey, Hans-Hilger Ropers

Journal:

Current Opinion in Genetics & Development

Year:

1995

Language:

english

File:

PDF, 400 KB

english, 1995

42

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

Clive J. Petry, Ken K. Ong, Dianne L. Wingate, James Brown, Carolyn D. Scott, The ALSPAC Study Team, E. Yvonne Jones, Marcus E. Pembrey, David B. Dunger

Journal:

Growth Hormone & IGF Research

Year:

2005

Language:

english

File:

PDF, 144 KB

english, 2005

43

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

Ian P Hall, John D Blakey, Khalid A Al Balushi, Amanda Wheatley, Ian Sayers, Marcus E Pembrey, Susan M Ring, Wendy L McArdle, David P Strachan

Journal:

Year:

2006

Language:

english

File:

PDF, 172 KB

english, 2006

44

Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes

Kristina Casteels, Ken Ong, David Phillips, Holly Bendall, Marcus Pembrey, Jo Poulton, David Dunger

Journal:

Year:

1999

Language:

english

File:

PDF, 71 KB

english, 1999

45

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

Adrian Vella, Jason D. Cooper, Christopher E. Lowe, Neil Walker, Sarah Nutland, Barry Widmer, Richard Jones, Susan M. Ring, Wendy McArdle, Marcus E. Pembrey, David P. Strachan, David B. Dunger, C.J. R

Journal:

The American Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 259 KB

english, 2005

46

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

Michael N. Weedon, Vanessa J. Clark, Yudong Qian, Yoav Ben-Shlomo, Nicholas Timpson, Shah Ebrahim, Debbie A. Lawlor, Marcus E. Pembrey, Susan Ring, Terry J. Wilkin, Linda D. Voss, Alison N. Jeffery, B

Journal:

The American Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 396 KB

english, 2006

47

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

Rachel M. Freathy, Michael N. Weedon, Amanda Bennett, Elina Hyppönen, Caroline L. Relton, Beatrice Knight, Beverley Shields, Kirstie S. Parnell, Christopher J. Groves, Susan M. Ring, Marcus E. Pembrey

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 210 KB

english, 2007

48

Fragile X mental retardation: current controversies

Marcus E. Pembrey, Robin M. Winter, Kay E. Davies

Journal:

Trends in Neurosciences

Year:

1986

Language:

english

File:

PDF, 652 KB

english, 1986

49

The burden of disease associated with filaggrin mutations: A population-based, longitudinal birth cohort study

Henderson, John, Northstone, Kate, Lee, Simon P., Liao, Haihui, Zhao, Yiwei, Pembrey, Marcus, Mukhopadhyay, Somnath, Smith, George Davey, Palmer, Colin N.A., McLean, W. H. Irwin, Irvine, Alan D.

Journal:

Journal of Allergy and Clinical Immunology

Year:

2008

Language:

english

File:

PDF, 231 KB

english, 2008

50

Mannose-binding lectin alleles in a prospectively recruited UK population

Richard Mead, Dominic Jack, Marcus Pembrey, Linda Tyfield, Malcolm Turner

Journal:

Year:

1997

Language:

english

File:

PDF, 58 KB

english, 1997