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Dr Beate St Pourcain

Dr Beate St Pourcain

Dr Beate St Pourcain
M.Sc., Ph.D.(Cardiff)

Honorary Lecturer

Oakfield House,
Oakfield Grove, Clifton BS8 2BN
(See a map)

Research summary

Beate St.Pourcain (nee Glaser) is a lecturer in Genetic Epidemiology within the School of Oral and Dental Sciences and affiliated with the MRC Integrative Epidemiology Unit. Her interests are the genetic underpinnings of neuro-developmental and developmental phenotypes. This includes autism and autistic traits, early language development and cleft lip and/or palate, where aetiological factors are likely to play a role very early during development. She is leading the genetic research of the Cleft Collective Cohort Studies, a large collection of patients with CL/P and their families, and is involved in the analysis of Next-Generation sequencing data as ...

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Biography

Lecturer in Genetic Epidemiology

ORDS, University of Bristol

2012 – Present

 

Research Associate

SSCM, University of Bristol

2007 – 2012

 

Post-doctoral Research Officer

Biostatistics and Bioinformatics Unit, Cardiff University

2006 – 2007

 

Post-doctoral Research Officer

Department of Psychological Medicine, Cardiff University

2005 – 2006

 

Part-time MSc in Genetic Epidemiology and Bioinformatics

Supervisor Peter Holmans

Cardiff University

2005 – 2007

 

PhD in Psychological Medicine

Supervisor Mike Owen

Cardiff University

2000 – 2005

 

Degree+MSc in Biology

University of Göttingen, Germany

1992 – 1999

 

Degree+MSc in Psychology

University of Göttingen, Germany

1992 – 1999

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Recent publications

  • Grove, J, Ripke, S, Als, TD, Mattheisen, M, Walters, RK, Won, H, Pallesen, J, Agerbo, E, Andreassen, OA, Anney, R, Awashti, S, Belliveau, R, Bettella, F, Buxbaum, JD, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Christensen, JH, Churchhouse, C, Dellenvall, K, Demontis, D, De Rubeis, S, Devlin, B, Djurovic, S, Dumont, AL, Goldstein, JI, Hansen, CS, Hauberg, ME, Hollegaard, MV, Hope, S, Howrigan, DP, Huang, H, Hultman, CM, Klei, L, Maller, J, Martin, J, Pedersen, CB, Smith, GD, St Pourcain, B & others 2019, ‘Identification of common genetic risk variants for autism spectrum disorder’. Nature Genetics, vol 51., pp. 431-444
  • , , , Demontis, D, Walters, RK, Martin, J, Mattheisen, M, Als, TD, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, JI, Grasby, KL, Grove, J, Gudmundsson, OO, Hansen, CS, Hauberg, ME, Hollegaard, MV, Howrigan, DP, Huang, H, Maller, JB, Martin, AR, Martin, NG, Moran, J, Pallesen, J, Palmer, DS, Pedersen, CB, Pedersen, MG, Poterba, T, Poulsen, JB, Ripke, S, Robinson, EB & others 2019, ‘Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder’. Nature Genetics, vol 51., pp. 63-75

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View complete publications list in the University of Bristol publications system

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