C
Caroline Crombie
Researcher at University of Aberdeen
Publications - 21
Citations - 11220
Caroline Crombie is an academic researcher from University of Aberdeen. The author has contributed to research in topics: Population & Haplotype. The author has an hindex of 18, co-authored 21 publications receiving 10595 citations. Previous affiliations of Caroline Crombie include Royal Cornhill Hospital & Aberdeen Royal Infirmary.
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Journal ArticleDOI
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Shaun Purcell,Shaun Purcell,Naomi R. Wray,Jennifer Stone,Jennifer Stone,Peter M. Visscher,Michael Conlon O'Donovan,Patrick F. Sullivan,Pamela Sklar,Pamela Sklar,Douglas M. Ruderfer,Andrew McQuillin,Derek W. Morris,Colm O'Dushlaine,Aiden Corvin,Peter Holmans,Stuart MacGregor,Hugh Gurling,Douglas Blackwood,Nicholas John Craddock,Michael Gill,Christina M. Hultman,Christina M. Hultman,George Kirov,Paul Lichtenstein,Walter J. Muir,Michael John Owen,Carlos N. Pato,Edward M. Scolnick,Edward M. Scolnick,David St Clair,Nigel Williams,Lyudmila Georgieva,Ivan Nikolov,Nadine Norton,Hywel Williams,Draga Toncheva,Vihra Milanova,Emma Flordal Thelander,Patrick Sullivan,Elaine Kenny,Emma M. Quinn,Khalid Choudhury,Susmita Datta,Jonathan Pimm,Srinivasa Thirumalai,Vinay Puri,Robert Krasucki,Jacob Lawrence,Digby Quested,Nicholas Bass,Caroline Crombie,Gillian Fraser,Soh Leh Kuan,Nicholas Walker,Kevin A. McGhee,Ben S. Pickard,P. Malloy,Alan W Maclean,Margaret Van Beck,Michele T. Pato,Helena Medeiros,Frank A. Middleton,Célia Barreto Carvalho,Christopher P. Morley,Ayman H. Fanous,David V. Conti,James A. Knowles,Carlos Ferreira,António Macedo,M. Helena Azevedo,Andrew Kirby,Andrew Kirby,Manuel A. R. Ferreira,Manuel A. R. Ferreira,Mark J. Daly,Mark J. Daly,Kimberly Chambert,Finny G Kuruvilla,Stacey Gabriel,Kristin G. Ardlie,Jennifer L. Moran +81 more
TL;DR: The extent to which common genetic variation underlies the risk of schizophrenia is shown, using two analytic approaches, and the major histocompatibility complex is implicate, which is shown to involve thousands of common alleles of very small effect.
Journal ArticleDOI
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson,Dan Rujescu,Sven Cichon,Olli Pietiläinen,Andres Ingason,Stacy Steinberg,Ragnheidur Fossdal,Engilbert Sigurdsson,Thordur Sigmundsson,Jacobine E. Buizer-Voskamp,Thomas Hansen,Thomas Hansen,Klaus D. Jakobsen,Klaus D. Jakobsen,Pierandrea Muglia,Clyde Francks,Paul M. Matthews,Arnaldur Gylfason,Bjarni V. Halldorsson,Daniel F. Gudbjartsson,Thorgeir E. Thorgeirsson,Asgeir Sigurdsson,Adalbjorg Jonasdottir,Aslaug Jonasdottir,Asgeir Björnsson,Sigurborg Mattiasdottir,Thorarinn Blondal,Magnús Haraldsson,Brynja B. Magnusdottir,Ina Giegling,Hans-Jürgen Möller,Annette M. Hartmann,Kevin V. Shianna,Dongliang Ge,Anna C. Need,Caroline Crombie,Gillian Fraser,Nicholas Walker,Jouko Lönnqvist,Jaana Suvisaari,Annamarie Tuulio-Henriksson,Tiina Paunio,T. Toulopoulou,Elvira Bramon,Marta Di Forti,Robin M. Murray,Mirella Ruggeri,Evangelos Vassos,Sarah Tosato,Muriel Walshe,Tao Li,Tao Li,Catalina Vasilescu,Thomas W. Mühleisen,August G. Wang,Henrik Ullum,Srdjan Djurovic,Ingrid Melle,Jes Olesen,Lambertus A. Kiemeney,Barbara Franke,Chiara Sabatti,Nelson B. Freimer,Jeffrey R. Gulcher,Unnur Thorsteinsdottir,Augustine Kong,Ole A. Andreassen,Roel A. Ophoff,Roel A. Ophoff,Alexander Georgi,Marcella Rietschel,Thomas Werge,Hannes Petursson,David Goldstein,Markus M. Nöthen,Leena Peltonen,Leena Peltonen,David A. Collier,David A. Collier,David St Clair,Kari Stefansson,Kari Stefansson +81 more
TL;DR: In a genome-wide search for CNVs associating with schizophrenia, a population-based sample was used to identify de novo CNVs by analysing 9,878 transmissions from parents to offspring and three deletions significantly associate with schizophrenia and related psychoses in the combined sample.
Journal ArticleDOI
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer Stone,Jennifer Stone,Jennifer Stone,Michael Conlon O'Donovan,Hugh Gurling,George Kirov,Douglas Blackwood,Aiden Corvin,Nicholas John Craddock,Michael Gill,Christina M. Hultman,Christina M. Hultman,Paul Lichtenstein,Andrew McQuillin,Carlos N. Pato,Douglas M. Ruderfer,Douglas M. Ruderfer,Douglas M. Ruderfer,Michael John Owen,David St Clair,Patrick F. Sullivan,Pamela Sklar,Pamela Sklar,Pamela Sklar,Shaun Purcell,Shaun Purcell,Shaun Purcell,Joshua M. Korn,Joshua M. Korn,Stuart MacGregor,Derek W. Morris,Colm O'Dushlaine,Mark J. Daly,Mark J. Daly,Mark J. Daly,Peter M. Visscher,Peter Holmans,Edward M. Scolnick,Edward M. Scolnick,Nigel Williams,Lucy Georgieva,Ivan Nikolov,Nadine Norton,Hywel Williams,Draga Toncheva,Vihra Milanova,Emma Flordal Thelander,Patrick Sullivan,Elaine Kenny,John L. Waddington,Khalid Choudhury,Susmita Datta,Jonathan Pimm,Srinivasa Thirumalai,Vinay Puri,Robert Krasucki,Jacob Lawrence,Digby Quested,Nicholas Bass,David Curtis,Caroline Crombie,Gillian Fraser,Soh Leh Kwan,Nicholas Walker,Walter J. Muir,Kevin A. McGhee,Ben S. Pickard,P. Malloy,Alan W Maclean,Margaret Van Beck,Michele T. Pato,Helena Medeiros,Frank A. Middleton,Célia Barreto Carvalho,Christopher P. Morley,Ayman H. Fanous,David V. Conti,James A. Knowles,Carlos Ferreira,António Macedo,M. Helena Azevedo,Steve McCarroll,Steve McCarroll,Mark J. Daly,Mark J. Daly,Mark J. Daly,Kimberly Chambert,Kimberly Chambert,Casey Gates,Stacey Gabriel,Scott Mahon,Kristen Ardlie +91 more
TL;DR: A genome-wide survey of rare CNVs in 3,391 patients with schizophrenia and 3,181 ancestrally matched controls provides strong support for a model of schizophrenia pathogenesis that includes the effects of multiple rare structural variants, both genome- wide and at specific loci.
Journal ArticleDOI
Normative data for the HADS from a large non-clinical sample
TL;DR: In this paper, the authors provided normative data for the Hospital Anxiety Depression Scale (HADS) to assess the rarity of a given HADS score, and thus provide a useful supplement to existing cut-off scores.
Journal ArticleDOI
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population.
Hreinn Stefansson,Jane Sarginson,Augustine Kong,Phil Yates,Valgerdur Steinthorsdottir,Einar Gudfinnsson,Steinunn Gunnarsdottir,Nicholas Walker,Hannes Petursson,Caroline Crombie,Andres Ingason,Jeffrey R. Gulcher,Kari Stefansson,David St Clair +13 more
TL;DR: This direct replication of haplotype association in a second population further implicates NRG1 as a factor that contributes to the etiology of schizophrenia.