N
Nicola J. Camp
Researcher at University of Utah
Publications - 238
Citations - 8706
Nicola J. Camp is an academic researcher from University of Utah. The author has contributed to research in topics: Single-nucleotide polymorphism & Population. The author has an hindex of 46, co-authored 213 publications receiving 7772 citations. Previous affiliations of Nicola J. Camp include Intermountain Healthcare & University of Sheffield.
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Journal ArticleDOI
A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration
Zhenglin Yang,Nicola J. Camp,Hui Sun,Zongzhong Tong,Daniel Gibbs,D. Joshua Cameron,Haoyu Chen,Yu Zhao,Erik G. Pearson,Xi Li,Jeremy Chien,Andrew T. DeWan,Jennifer Harmon,Paul S. Bernstein,Viji Shridhar,Norman A. Zabriskie,Josephine Hoh,Kimberly A. Howes,Kang Zhang +18 more
TL;DR: A single-nucleotide polymorphism in the promoter region of HTRA1 is the most likely causal variant for AMD at 10q26 and is estimated to confer a population attributable risk of 49.3%.
Journal ArticleDOI
A candidate prostate cancer susceptibility gene at chromosome 17p.
Sean V. Tavtigian,Jacques Simard,David H. F. Teng,Vicki Abtin,Michelle Baumgard,Audrey Beck,Nicola J. Camp,Nicola J. Camp,Arlene Carillo,Yang Chen,Priya Dayananth,Marc Desrochers,Martine Dumont,James M. Farnham,David A. Frank,Cheryl Frye,Siavash Ghaffari,Jamila Gupte,Rong Hu,Diana Iliev,Teresa Janecki,Edward N. Kort,Kirsten Laity,Amber Leavitt,Gilles Leblanc,Jodi Mcarthur-Morrison,Amy Pederson,Brandon Penn,Kelly T. Peterson,Julia Reid,Sam Richards,Marianne Schroeder,Richard D. Smith,Sarah C. Snyder,Brad Swedlund,Jeff Swensen,Alun Thomas,Martine Tranchant,Ann Marie Woodland,Fernand Labrie,Mark H. Skolnick,Susan L. Neuhausen,Johanna M. Rommens,Lisa A. Cannon-Albright,Lisa A. Cannon-Albright +44 more
TL;DR: A genome-wide scan of large, high-risk pedigrees from Utah has provided evidence for linkage to a locus on chromosome 17p, identifying a gene, ELAC2, harboring mutations (including a frameshift and a nonconservative missense change) that segregate with prostate cancer in two pedigree.
Journal ArticleDOI
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women
Leila Dorling,Sara Carvalho,Jamie Allen,Anna González-Neira,Craig Luccarini,Cecilia Wahlström,Karen A. Pooley,Michael T. Parsons,Cristina Fortuno,Qin Wang,Manjeet K. Bolla,Joe Dennis,Renske Keeman,M. Rosario Alonso,Nuria Álvarez,Belen Herraez,Victoria Fernández,Rocio Núñez-Torres,Ana Osorio,Jeanette Valcich,Minerva Li,Therese Törngren,Patricia Harrington,Caroline Baynes,Don M. Conroy,Brennan Decker,Laura Fachal,Nasim Mavaddat,Thomas U. Ahearn,Kristiina Aittomäki,Natalia Antonenkova,Norbert Arnold,Patrick Arveux,Margreet G. E. M. Ausems,Päivi Auvinen,Heiko Becher,Matthias W. Beckmann,Sabine Behrens,Marina Bermisheva,Katarzyna Białkowska,Carl Blomqvist,Natalia Bogdanova,Nadja Bogdanova-Markov,Stig E. Bojesen,Bernardo Bonanni,Anne Lise Børresen-Dale,Hiltrud Brauch,Michael Bremer,Ignacio Briceño,Thomas Brüning,Barbara Burwinkel,David Cameron,Nicola J. Camp,Archie Campbell,Angel Carracedo,Jose E. Castelao,Melissa H. Cessna,Stephen J. Chanock,Hans Christiansen,J. Margriet Collée,Emilie Cordina-Duverger,Sten Cornelissen,Kamila Czene,Thilo Dörk,Arif B. Ekici,Christoph Engel,Mikael Eriksson,Peter A. Fasching,Jonine D. Figueroa,Henrik Flyger,Asta Försti,Marike Gabrielson,Manuela Gago-Dominguez,Vassilios Georgoulias,Fabián Gil,Graham G. Giles,Gord Glendon,Encarna B. Gomez Garcia,Grethe I. Grenaker Alnæs,Pascal Guénel,Andreas Hadjisavvas,Lothar Haeberle,Eric Hahnen,Per Hall,Ute Hamann,Elaine F. Harkness,Jaana M. Hartikainen,Mikael Hartman,Wei He,Bernadette A M Heemskerk-Gerritsen,Peter Hillemanns,Frans B. L. Hogervorst,Antoinette Hollestelle,Weang Kee Ho,Maartje J. Hooning,Anthony Howell,Keith Humphreys,Faiza Idris,Anna Jakubowska,Audrey Y. Jung,Pooja Middha Kapoor,Michael J. Kerin,Elza Khusnutdinova,Sung-Won Kim,Yon-Dschun Ko,Veli-Matti Kosma,Vessela N. Kristensen,Kyriacos Kyriacou,Inge M. M. Lakeman,Jong Won Lee,Min Hyuk Lee,Jingmei Li,Annika Lindblom,Wing-Yee Lo,Maria A. Loizidou,Artitaya Lophatananon,Jan Lubinski,Robert J. MacInnis,Michael J. Madsen,Arto Mannermaa,Mehdi Manoochehri,Siranoush Manoukian,Sara Margolin,Maria Elena Martinez,Tabea Maurer,Dimitrios Mavroudis,Catriona McLean,Alfons Meindl,Arjen R. Mensenkamp,Kyriaki Michailidou,Nicola Miller,Nur Aishah Taib,Kenneth Muir,Anna Marie Mulligan,Heli Nevanlinna,William G. Newman,Børge G. Nordestgaard,Pei-Sze Ng,Jan C. Oosterwijk,Sue K. Park,Tjoung-Won Park-Simon,Jose Ignacio Arias Perez,Paolo Peterlongo,David J. Porteous,Karolina Prajzendanc,Darya Prokofyeva,Paolo Radice,Muhammad Usman Rashid,Valerie Rhenius,Matti A. Rookus,Thomas Rüdiger,Emmanouil Saloustros,Elinor J. Sawyer,Rita K. Schmutzler,Andreas Schneeweiss,Peter Schürmann,Mitul Shah,Christof Sohn,Melissa C. Southey,Harald Surowy,Maija Suvanto,Somchai Thanasitthichai,Ian Tomlinson,Diana Torres,Thérèse Truong,Maria Tzardi,Yana Valova,Christi J. van Asperen,Rob M. van Dam,Ans M.W. van den Ouweland,Lizet E. van der Kolk,Elke M van Veen,Camilla Wendt,Justin A. Williams,Xiaohong R. Yang,Sook-Yee Yoon,M. Pilar Zamora,D. Gareth Evans,Miguel de la Hoya,Jacques Simard,Antonis C. Antoniou,Åke Borg,Irene L. Andrulis,Jenny Chang-Claude,Montserrat Garcia-Closas,Georgia Chenevix-Trench,Roger L. Milne,Paul D.P. Pharoah,Marjanka K. Schmidt,Amanda B. Spurdle,Maaike P.G. Vreeswijk,Javier Benitez,Alison M. Dunning,Anders Kvist,Soo Hwang Teo,Peter Devilee,Douglas F. Easton +196 more
TL;DR: The results of this study define the genes that are most clinically useful for inclusion on panels for the prediction of breast cancer risk, as well as provide estimates of the risks associated with protein-truncating variants, to guide genetic counseling.
Journal ArticleDOI
Interleukin-1 Receptor Antagonist Gene Polymorphism and Coronary Artery Disease
Sheila E. Francis,Nicola J. Camp,Rachael Dewberry,Julian Gunn,Petros Syrris,Nicholas D. Carter,Stephen Jeffery,Juan Carlos Kaski,David C. Cumberland,Gordon W. Duff,David C. Crossman +10 more
TL;DR: IL-1RN*2 was significantly associated with SVD, and a difference in genetic association between SVD and MVD was also apparent.