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Results 1 to 25 of 141

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The past, present, and future of direct-to-consumer genetic testsHELGASON, Agnar; STEFANSSON, Kári.Dialogues in clinical neuroscience. 2010, Vol 12, Num 1, pp 61-68, issn 1294-8322, 8 p.Article

Role of Pharmacogenomics in drug developmentHAKONARSSON, Hakon; STEFANSSON, Kari.Drug development research. 2004, Vol 62, Num 2, pp 86-96, issn 0272-4391, 11 p.Article

An Icelandic example of the impact of population structure on association studiesHELGASON, Agnar; YNGVADOTTIR, Bryndis; HRAFNKELSSON, Birgir et al.Nature genetics. 2005, Vol 37, Num 1, pp 90-95, issn 1061-4036, 6 p.Article

Assessing the signatures of selection in PRNP from polymorphism data : results support kreitman and Di Rienzo's opinionSOLDEVILA, Marta; CALAFELL, Francesc; HELGASON, Agnar et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 7, pp 389-391, issn 0168-9525, 3 p.Article

Segmental duplication density decrease with distance to human-mouse breaks of syntenySAINZ, Jesus; ROVENSKY, Pavol; GUDJONSSON, Sigurjon A et al.European journal of human genetics. 2006, Vol 14, Num 2, pp 216-221, issn 1018-4813, 6 p.Article

Neuregulin 1 and schizophreniaSTEFANSSON, Hreinn; STEINTHORSDOTTIR, Valgerdur; THORGEIRSSON, Thorgeir E et al.Annals of medicine (Helsinki). 2004, Vol 36, Num 1, pp 62-71, issn 0785-3890, 10 p.Article

Impact of Genetics on Low Bone Mass in AdultsSIGURDSSON, Gunnar; HALLDORSSON, Bjarni V; STYRKARSDOTTIR, Unnur et al.Journal of bone and mineral research (Print). 2008, Vol 23, Num 10, pp 1584-1590, issn 0884-0431, 7 p.Article

mtDNA and the islands of the North Atlantic: Estimating the proportions of norse and Gaelic ancestryHELGASON, Agnar; HICKEY, Eileen; GOODACRE, Sara et al.American journal of human genetics. 2001, Vol 68, Num 3, pp 723-737, issn 0002-9297Article

Familiality of kidney stone disease in IcelandEDVARDSSON, Vidar O; PALSSON, Runolfur; INDRIDASON, Olafur S et al.Scandinavian journal of urology and nephrology. 2009, Vol 43, Num 5, pp 420-424, issn 0036-5599, 5 p.Article

A populationwide coalescent analysis of Icelandic matrilineal and patrilineal genealogies: Evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomesHELGASON, Agnar; HRAFNKELSSON, Birgir; GULCHER, Jeffrey R et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1370-1388, issn 0002-9297, 19 p.Article

An Association Between the Kinship and Fertility of Human CouplesHELGASON, Agnar; PALSSON, Snaebjörn; GUÖBJARTSSON, Daniel F et al.Science (Washington, D.C.). 2008, Vol 319, Num 5864, pp 813-816, issn 0036-8075, 4 p.Article

Assessing population differentiation and isolation from single-nucleotide polymorphism dataNICHOLSON, George; SMITH, Albert V; JONSSON, Frosti et al.Journal of the Royal Statistical Society. Series B, statistical methodology. 2002, Vol 64, pp 695-715, issn 1369-7412, 21 p., 4Article

A Mouse Model that Recapitulates Cardinal Features of the 15q13.3 Microdeletion Syndrome Including Schizophrenia- and Epilepsy-Related AlterationsKIM FEJGIN; NIELSEN, Jacob; LARSEN, Peter H et al.Biological psychiatry (1969). 2014, Vol 76, Num 2, pp 128-137, issn 0006-3223, 10 p.Article

Rate of de novo mutations and the importance of father's age to disease riskKONG, Augustine; FRIGGE, Michael L; WONG, Wendy S. W et al.Nature (London). 2012, Vol 488, Num 7412, pp 471-475, issn 0028-0836, 5 p.Article

Genome-Wide Significant Association Between a Sequence Variant at 15q15.2 and Lung Cancer RiskRAFNAR, Thorunn; SULEM, Patrick; BJARNASON, Hjordis et al.Cancer research (Chicago, Ill.). 2011, Vol 71, Num 4, pp 1356-1361, issn 0008-5472, 6 p.Article

Identification of low-frequency variants associated with gout and serum uric acid levelsSULEM, Patrick; GUDBJARTSSON, Daniel F; MAGNUSSON, Gisli et al.Nature genetics. 2011, Vol 43, Num 11, pp 1127-1130, issn 1061-4036, 4 p.Article

Variant in the sequence of the LINGO1 gene confers risk of essential tremorSTEFANSSON, Hreinn; STEINBERG, Stacy; BÖTTCHER, Yvonne et al.Nature genetics. 2009, Vol 41, Num 3, pp 277-279, issn 1061-4036, 3 p.Article

Detection of sharing by descent, long-range phasing and haplotype imputationKONG, Augustine; MASSON, Gisli; SULEM, Patrick et al.Nature genetics. 2008, Vol 40, Num 9, pp 1068-1075, issn 1061-4036, 8 p.Article

Risk Variants for Atrial Fibrillation on Chromosome 4q25 Associate with Ischemic StrokeGRETARSDOTTIR, Solveig; THORLEIFSSON, Gudmar; BJARNASON, Hjordis et al.Annals of neurology. 2008, Vol 64, Num 4, pp 402-409, issn 0364-5134, 8 p.Article

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionHELGASON, Agnar; PALSSON, Snaebjörn; BENEDIKTSSON, Rafn et al.Nature genetics. 2007, Vol 39, Num 2, pp 218-225, issn 1061-4036, 8 p.Article

A common variant associated with prostate cancer in European and African populationsAMUNDADOTTIR, Laufey T; SULEM, Patrick; JAKOBSDOTTIR, Margret et al.Nature genetics. 2006, Vol 38, Num 6, pp 652-658, issn 1061-4036, 7 p.Article

Recombination rate and reproductive success in humansKONG, Augustine; BARNARD, John; LAMB, Neil E et al.Nature genetics. 2004, Vol 36, Num 11, pp 1203-1206, issn 1061-4036, 4 p.Article

Genomewide scan for hand osteoarthritis: A novel mutation in matrilin-3STEFANSSON, Stefan Einar; JONSSON, Helgi; KONG, Augustine et al.American journal of human genetics. 2003, Vol 72, Num 6, pp 1448-1459, issn 0002-9297, 12 p.Article

The natural history of untreated multiple sclerosis in Iceland. A total population-based 50 year prospective studyBENEDIKZ, John; STEFANSSON, Magnus; GUOMUNDSSON, Julius et al.Clinical neurology and neurosurgery. 2002, Vol 104, Num 3, pp 208-210, issn 0303-8467Conference Paper

Variant of TREM2 Associated with the Risk of Alzheimer's DiseaseJONSSON, Thorlakur; STEFANSSON, Hreinn; RUJESCU, Dan et al.The New England journal of medicine. 2013, Vol 368, Num 2, pp 107-116, issn 0028-4793, 10 p.Article

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