P
P.F. Sullivan
Researcher at University of North Carolina at Chapel Hill
Publications - 28
Citations - 929
P.F. Sullivan is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Population & Genome-wide association study. The author has an hindex of 14, co-authored 27 publications receiving 798 citations. Previous affiliations of P.F. Sullivan include Karolinska Institutet.
Papers
More filters
Journal ArticleDOI
Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions.
Solveig K. Sieberts,Thanneer M. Perumal,Minerva M. Carrasquillo,Mariet Allen,Joseph S. Reddy,Gabriel E. Hoffman,Kristen K. Dang,John N. Calley,Phillip J. Ebert,James A. Eddy,Xue Wang,Anna K. Greenwood,Sara Mostafavi,Sara Mostafavi,S Akbarian,J Bendl,M S Breen,K Brennand,L Brown,A Browne,J D Buxbaum,A Charney,Andrew Chess,Couto L,Gregory E. Crawford,Devillers O,Bernie Devlin,Amanda Dobbyn,E Domenici,M Filosi,E Flatow,Nancy Francoeur,John F. Fullard,S E Gil,Kiran Girdhar,A Gulyás-Kovács,R.E. Gur,C G Hahn,Vahram Haroutunian,Mads E. Hauberg,Laura M. Huckins,Rivka Jacobov,Y Jiang,Jessica S. Johnson,Bibi Kassim,Y Kim,Lambertus Klei,Robin Kramer,Mario Lauria,Thomas Lehner,David A. Lewis,Barbara K. Lipska,Kelsey S. Montgomery,R Park,C Rosenbluh,Panagiotis Roussos,Douglas M. Ruderfer,G Senthil,Hardik Shah,Laura G. Sloofman,L Song,E Stahl,P.F. Sullivan,R Visintainer,J Wang,Y C Wang,Jennifer Wiseman,E Xia,W Zhang,Elizabeth Zharovsky,L Addis,S N Addo,David C. Airey,Matthias Arnold,David A. Bennett,Y Bi,K Biber,Colette Blach,E Bradhsaw,Paul Brennan,R Canet-Aviles,S Cao,A Cavalla,Yooree Chae,W W Chen,J Cheng,David A. Collier,J L Dage,Eric B. Dammer,J W Davis,John B. Davis,Derek Drake,D Duong,Brian J. Eastwood,Michelle E. Ehrlich,B Ellingson,B W Engelmann,S Esmaeelinieh,Daniel Felsky,Cory C. Funk,Chris Gaiteri +100 more
TL;DR: A colocalization analysis is applied to identify genes underlying the GWAS association peaks for schizophrenia and identify a potentially novel gene colocalized with lncRNA RP11-677M14.
Journal ArticleDOI
Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4
Carol A. Prescott,Carol A. Prescott,P.F. Sullivan,Po-Hsiu Kuo,Bradley T. Webb,J. Vittum,Diana G. Patterson,Dawn L. Thiselton,John Myers,M. Devitt,Lisa Halberstadt,V.P. Robinson,Michael C. Neale,E J C G van den Oord,Declan Walsh,Brien P. Riley,Kenneth S. Kendler +16 more
TL;DR: The results of this study suggest the importance of genetic variation in chromosome 4 in the etiology and severity of alcoholism in Caucasian populations.
Journal ArticleDOI
Stitching the synapse: Cross-linking mass spectrometry into resolving synaptic protein interactions
Miguel A. Gonzalez-Lozano,Frank Koopmans,P.F. Sullivan,P.F. Sullivan,Jonas Protze,Gerd Krause,Matthijs Verhage,Ka Wan Li,Fan Liu,August B. Smit +9 more
TL;DR: This work made use of recent advances in cross-linking mass spectrometry (XL-MS) in combination with biochemical and computational approaches to reveal the architecture and assembly of synaptic protein complexes from mouse brain hippocampus and cerebellum.
Journal ArticleDOI
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility
Ming Li,Ming Li,Xiong-Jian Luo,Marcella Rietschel,Marcella Rietschel,Cathryn M. Lewis,Manuel Mattheisen,Bertram Müller-Myhsok,Stéphane Jamain,Marion Leboyer,Mikael Landén,Mikael Landén,Paul M. Thompson,Sven Cichon,Markus M. Nöthen,Markus M. Nöthen,Thomas G. Schulze,Thomas G. Schulze,P.F. Sullivan,Sarah E. Bergen,Sarah E. Bergen,Gary Donohoe,Derek W. Morris,April Hargreaves,Michael Gill,Aiden Corvin,Christina M. Hultman,Arthur W. Toga,Lei Shi,Qiang Lin,Huiqing Shi,Lin Gan,Andreas Meyer-Lindenberg,Darina Czamara,C. Henry,Bruno Etain,J. C. Bis,Mohammad Arfan Ikram,Myriam Fornage,Stéphanie Debette,Stéphanie Debette,Lenore J. Launer,Sudha Seshadri,Sudha Seshadri,Susanne Erk,Henrik Walter,Henrik Walter,A. Heinz,Frank Bellivier,Jason L. Stein,Sarah E. Medland,Sarah E. Medland,Alejandro Arias Vasquez,Derrek P. Hibar,Barbara Franke,Nicholas G. Martin,Margaret J. Wright,Bing Su +57 more
TL;DR: The results suggest that differential population histories due to natural selection on regional populations may lead to genetic heterogeneity of susceptibility to complex diseases, such as BD, and explain inconsistencies in detecting the genetic markers of these diseases among different ethnic populations.
Journal ArticleDOI
The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects.
Wouter J. Peyrot,Sang Hong Lee,Yuri Milaneschi,Abdel Abdellaoui,Enda M. Byrne,Tõnu Esko,Tõnu Esko,Tõnu Esko,E.J.C. de Geus,Gibran Hemani,Gibran Hemani,Jouke-Jan Hottenga,Stefan Kloiber,Douglas F. Levinson,Susanne Lucae,Nicholas G. Martin,S. E. Medland,Andres Metspalu,Andres Metspalu,L. Milani,L. Milani,Markus M. Noethen,James B. Potash,M. Rietschel,Cornelius A. Rietveld,Stephan Ripke,Jing Shi,Gonneke Willemsen,Zhihong Zhu,Dorret I. Boomsma,Naomi R. Wray,Brenda W.J.H. Penninx,C. M. Lewis,S. P. Hamilton,M. M. Weissman,Gerome Breen,D. H. R. Blackwood,Sven Cichon,A. C. Heath,Florian Holsboer,P. A. F. Madden,P. McGuffin,P. Muglia,Michele L. Pergadia,Danyu Lin,Bertram Müller-Myhsok,Stacy Steinberg,Hans-Jörgen Grabe,P. Lichtenstein,Patrik K. E. Magnusson,Roy H. Perlis,M. Preisig,Jordan W. Smoller,K. Stefansson,Rudolf Uher,Z. Kutalik,Katherine E. Tansey,A. Teumer,Alexander Viktorin,Michael R. Barnes,Thomas Bettecken,Elisabeth B. Binder,René Breuer,Victor M. Castro,Susanne Churchill,William Coryell,N. Craddock,Ian W. Craig,Darina Czamara,Franziska Degenhardt,A. E. Farmer,Maurizio Fava,John Frank,Vivian S. Gainer,Patience J. Gallagher,S.D. Gordon,Sergey Goryachev,Marcela González Gross,Michel Guipponi,Anjali K. Henders,Stefan Herms,Ian B. Hickie,Susanne Hoefels,Witte J.G. Hoogendijk,Dan V. Iosifescu,Marcus Ising,I. Jones,L. A. Jones,T. Jung-Ying,James A. Knowles,Isaac S. Kohane,Martin A. Kohli,Ania Korszun,Mikael Landén,William Lawson,Guy Lewis,Donald J. MacIntyre,W. Maier,Manuel Mattheisen,Patrick J. McGrath,Andrew M. McIntosh,Alan W. McLean,Christel M. Middeldorp,Lefkos T. Middleton,G. M. Montgomery,Shawn N. Murphy,Matthias Nauck,Willem A. Nolen,Dale R. Nyholt,Michael Conlon O'Donovan,Hogni Oskarsson,N. L. Pedersen,William A. Scheftner,Andrea Schulz,Thomas G. Schulze,Stanley I. Shyn,Emil L. Sigurdsson,Susan L. Slager,J.H. Smit,Hreinn Stefansson,Michael Steffens,Thorgeir E. Thorgeirsson,Federica Tozzi,Jens Treutlein,Manfred Uhr,E. J. C. G. van den Oord,G van Grootheest,Henry Völzke,Jeffrey B. Weilburg,Frans G. Zitman,Neale Bm,M. Daly,P.F. Sullivan,Arpana Agrawal,Eva Albrecht,Behrooz Z. Alizadeh,Jüri Allik,Najaf Amin,John Attia,Stefania Bandinelli,John Barnard,Franois Bastardot,Sebastian E. Baumeister,Jonathan P. Beauchamp,Daniel J. Benjamin,Kelly S. Benke,David A. Bennett,Klaus Berger,Lawrence F. Bielak,Laura J. Bierut,Jeffrey A. Boatman,Patricia A. Boyle,Ute Bültmann,Harry Campbell,David Cesarini,Christopher F. Chabris,Lynn Cherkas,Mina K. Chung,Dalton Conley,Francesco Cucca,George Davey-Smith,Gail Davies,Mariza de Andrade,Philip L. De Jager,Christiaan de Leeuw,Jan-Emmanuel De Neve,Ian J. Deary,George Dedoussis,Panos Deloukas,Jaime Derringer,Maria Dimitriou,Gudny Eiriksdottir,Niina Eklund,Martin F. Elderson,Johan G. Eriksson,Daniel S. Evans,David M. Evans,Jessica D. Faul,Rudolf S N Fehrmann,Luigi Ferrucci,Krista Fischer,Lude Franke,Melissa E. Garcia,Christian Gieger,Hkon K. Gjessing,Patrick J. F. Groenen,Henrik Grönberg,Vilmundur Gudnason,Sara Hägg,Per Hall,Jennifer R. Harris,Juliette Harris,Tamara B. Harris,Nicholas D. Hastie,Caroline Hayward,Andrew Heath,Dena G. Hernandez,W. Hoffmann,Adriaan Hofman,Albert Hofman,Rolf Holle,Elizabeth G. Holliday,Christina Holzapfel,William G. Iacono,Carla A. Ibrahim-Verbaas,Thomas Illig,Erik Ingelsson,Bo Jacobsson,Marjo-Riitta Järvelin,Min A. Jhun,Magnus Johannesson,Peter K. Joshi,Astanand Jugessur,Marika Kaakinen,Mika Kähönen,Stavroula Kanoni,J Kaprio,Sharon L.R. Kardia,Juha Karjalainen,Robert M. Kirkpatrick,Philipp Koellinger,Ivana Kolcic,Matthew Kowgier,Kati Kristiansson,Robert F. Krueger,Zoltán Kutalik,Jari Lahti,David Laibson,Antti Latvala,Lenore J. Launer,Debbie A Lawlor,Terho Lethimäki,Jingmei Li,Paul Lichtenstein,Peter Lichtner,David C. Liewald,Peng Lin,Penelope A. Lind,Yongmei Liu,Kurt Lohman,Marisa Loitfelder,Pamela A. F. Madden,Patrick K.E. Magnusson,Tomi E. Mäkinen,Pedro Marques Vidal,Nicolas W. Martin,Marco Masala,Matt McGue,George McMahon,Osorio Meirelles,Michelle N. Meyer,Andreas Mielck,Lili Milani,Lili Milani,Michael B. Miller,Grant W. Montgomery,Sutapa Mukherjee,Ronny Myhre,Marja-Liisa Nuotio,Christopher Oldmeadow,Ben A. Oostra,Lyle J. Palmer,Aarno Palotie,Markus Perola,K. Petrovic,Patricia A. Peyser,Ozren Polasek,Danielle Posthuma,Martin Preisig,Lydia Quaye,Katri Räikkönen,Olli T. Raitakari,Anu Realo,Eva Reinmaa,John P. Rice,Susan M. Ring,Samuli Ripatti,Fernando Rivadeneira,Thais S. Rizzi,Igor Rudan,Aldo Rustichini,Veikko Salomaa,Antti-Pekka Sarin,David Schlessinger,Helena Schmidt,Reinhold E. Schmidt,Rodney J. Scott,Konstantin Shakhbazov,Albert V. Smith,Jennifer A. Smith,Harold Snieder,Beate St Pourcain,John M. Starr,Jae Hoon Sul,Ida Surakka,Rauli Svento,Toshiko Tanaka,Antonio Terracciano,Alexander Teumer,Roy Thurik,Henning Tiemeier,Nicholas J. Timpson,André G. Uitterlinden,Matthijs J. H. M. van der Loos,Cornelia M. van Duijn,Frank J. A. van Rooij,David R. Van Wagoner,Erkki Vartiainen,Jorma Viikari,Peter M. Visscher,Veronique Vitart,Peter Vollenweider,Henry Völzke,Judith M. Vonk,Gérard Waeber,David R. Weir,Jürgen Wellmann,Harm-Jan Westra,H.-Erich Wichmann,Elisabeth Widen,James F. Wilson,Alan F. Wright,Jian Yang,Lei Yu,Wei Zhao +324 more
TL;DR: An association of lower EA and MDD risk is confirmed, but this association was not because of measurable pleiotropic genetic effects, which suggests that environmental factors could be involved, for example, socioeconomic status.