O
Outi Vierimaa
Researcher at Oulu University Hospital
Publications - 25
Citations - 4513
Outi Vierimaa is an academic researcher from Oulu University Hospital. The author has contributed to research in topics: Germline mutation & MEN1. The author has an hindex of 20, co-authored 25 publications receiving 4222 citations. Previous affiliations of Outi Vierimaa include University of Oulu.
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Journal ArticleDOI
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
Ian Tomlinson,Alam Na,Andrew Rowan,Ella Barclay,Emma Jaeger,David P. Kelsell,Irene M. Leigh,Gorman P,H. Lamlum,Shamima Rahman,Roylance Rr,Simon E. Olpin,Steve Bevan,Karen Barker,N Hearle,Richard S. Houlston,Maija Ht Kiuru,Rainer Lehtonen,Auli Karhu,Susa Vilkki,Päivi Laiho,Eklund C,Outi Vierimaa,Kristiina Aittomäki,Marja Hietala,Pertti Sistonen,Anders Paetau,Reijo Salovaara,Riitta Herva,Launonen,Lauri A. Aaltonen +30 more
TL;DR: It is shown that a gene that predisposes to multiple fibroids, cutaneous leiomyomata and renal cell carcinoma is mapped to chromosome 1q42, and that this gene encodes fumarate hydratase, an enzyme of the tricarboxylic acid cycle.
Journal ArticleDOI
Inherited susceptibility to uterine leiomyomas and renal cell cancer
Virpi Launonen,Outi Vierimaa,Maija Ht Kiuru,Jorma Isola,Stina Roth,Eero Pukkala,Pertti Sistonen,Riitta Herva,Lauri A. Aaltonen +8 more
TL;DR: It is shown that predisposition to uterine leiomyomas and papillary renal cell cancer can be inherited dominantly through the hereditaryLeiomyomatosis and renal cell cancers (HLRCC) gene.
Journal ArticleDOI
Pituitary Adenoma Predisposition Caused by Germline Mutations in the AIP Gene
Outi Vierimaa,Marianthi Georgitsi,Rainer Lehtonen,Pia Vahteristo,Antti Kokko,Anniina Raitila,Karoliina Tuppurainen,Tapani Ebeling,Pasi I. Salmela,Ralf Paschke,Sadi Gundogdu,Ernesto De Menis,Markus J. Mäkinen,Virpi Launonen,Auli Karhu,Lauri A. Aaltonen +15 more
TL;DR: Combining chip-based technologies with genealogy data, germline mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene in individuals with pituitary adenoma predisposition (PAP) are identified.
Journal ArticleDOI
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study
Adrian Daly,Maria A. Tichomirowa,Patrick Petrossians,Elina Heliövaara,Marie Lise Jaffrain-Rea,Anne Barlier,Luciana Ansaneli Naves,Tapani Ebeling,Auli Karhu,Antti Raappana,Laure Cazabat,Ernesto De Menis,Carmen Fajardo Montañana,Gérald Raverot,Robert J. Weil,Timo Sane,Dominique Maiter,Sebastian J C M M Neggers,Maria Yaneva,AntoineAntoine Tabarin,Elisa Verrua,Eija Eloranta,Arnaud Murat,Outi Vierimaa,Pasi I. Salmela,Philippe Emy,Rodrigo A. Toledo,Maria Isabel Sabaté,Chiara Villa,Chiara Villa,Marc Popelier,Roberto Salvatori,Juliet Jennings,Ángel Ferrández Longás,José Ignacio Labarta Aizpún,Marianthi Georgitsi,Ralf Paschke,Cristina L. Ronchi,Matti Välimäki,Carola Saloranta,Wouter W. de Herder,Renato Cozzi,Mirtha Guitelman,Flavia Magri,Maria Stefania Lagonigro,Georges Halaby,Vinciane Corman,Marie-Thérèse Hagelstein,Jean-Francis Vanbellinghen,Gustavo Barcelos Barra,Anne-Paule Gimenez-Roqueplo,Fergus J. Cameron,Françoise Borson-Chazot,Ian M. Holdaway,Sergio P. A. Toledo,Günter K. Stalla,Anna Spada,Sabina Zacharieva,Jérôme Bertherat,Thierry Brue,Vincent Bours,Philippe Chanson,Lauri A. Aaltonen,Albert Beckers +63 more
TL;DR: Prisposition for aggressive disease in young patients, often in a familial setting, suggests that earlier diagnosis of AIPmut pituitary adenomas may have clinical utility.
Journal ArticleDOI
Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.
Marianthi Georgitsi,Anniina Raitila,Auli Karhu,Rob B. van der Luijt,Cora M. Aalfs,Timo Sane,Outi Vierimaa,Markus J. Mäkinen,Karoliina Tuppurainen,Ralph Paschke,Oliver Gimm,Christian A. Koch,Sadi Gundogdu,Anneke Lucassen,Marc Tischkowitz,Louise Izatt,Simon Aylwin,Gul Bano,Shirley Hodgson,Ernesto De Menis,Virpi Launonen,Pia Vahteristo,Lauri A. Aaltonen +22 more
TL;DR: The results support the previous finding that germline CDKN1B/p27(Kip1) mutations predispose to a human MEN1-like condition.