PubMed

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

Zhao J, Bradfield JP, Zhang H, Annaiah K, Wang K, Kim CE, Glessner JT, Frackelton EC, Otieno FG, Doran J, Thomas KA, Garris M, Hou C, Chiavacci RM, Li M, Berkowitz RI, Hakonarson H, Grant SF.

Diabetes. 2009 Nov 23. [Epub ahead of print]PMID: 19933996 [PubMed - as supplied by publisher]

Common variants at five new loci associated with early-onset inflammatory bowel disease.

Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, Kugathasan S, Bradfield JP, Walters TD, Sleiman P, Kim CE, Muise A, Wang K, Glessner JT, Saeed S, Zhang H, Frackelton EC, Hou C, Flory JH, Otieno G, Chiavacci RM, Grundmeier R, Castro M, Latiano A, Dallapiccola B, Stempak J, Abrams DJ, Taylor K, McGovern D; Western Regional Research Alliance for Pediatric IBD; International IBD Genetics Consortium, Heyman MB, Ferry GD, Kirschner B, Lee J, Essers J, Grand R, Stephens M, Levine A, Piccoli D, Van Limbergen J, Cucchiara S, Monos DS, Guthery SL, Denson L, Wilson DC, Grant SF, Daly M, Silverberg MS, Satsangi J, Hakonarson H.

Nat Genet. 2009 Dec;41(12):1335-40. Epub 2009 Nov 15.PMID: 19915574 [PubMed - in process]Related articles

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

Wei Z, Wang K, Qu HQ, Zhang H, Bradfield J, Kim C, Frackleton E, Hou C, Glessner JT, Chiavacci R, Stanley C, Monos D, Grant SF, Polychronakos C, Hakonarson H.

PLoS Genet. 2009 Oct;5(10):e1000678. Epub 2009 Oct 9.PMID: 19816555 [PubMed - in process]Related articlesFree article

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry.

Flory JH, Sleiman PM, Christie JD, Annaiah K, Bradfield J, Kim CE, Glessner J, Imielinski M, Li H, Frackelton EC, Cuiping H, Otieno G, Thomas K, Smith R, Glaberson W, Garris M, Chiavacci R, Allen J, Spergel J, Grundmeier R, Grunstein M, Magnusson M, Grant SF, Bønnelykke K, Bisgaard H, Hakonarson H.

J Allergy Clin Immunol. 2009 Sep;124(3):605-7. Epub 2009 Aug 5. No abstract available. PMID: 19660801 [PubMed - indexed for MEDLINE]Related articles

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

Grant SF, Wang K, Zhang H, Glaberson W, Annaiah K, Kim CE, Bradfield JP, Glessner JT, Thomas KA, Garris M, Frackelton EC, Otieno FG, Chiavacci RM, Nah HD, Kirschner RE, Hakonarson H.

J Pediatr. 2009 Dec;155(6):909-13. Epub 2009 Aug 4.PMID: 19656524 [PubMed - in process]Related articles

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, Medne L, Annaiah K, Bradfield JP, Dabaghyan E, Eckert A, Onyiah CC, Ostapenko S, Otieno FG, Santa E, Shaner JL, Skraban R, Smith RM, Elia J, Goldmuntz E, Spinner NB, Zackai EH, Chiavacci RM, Grundmeier R, Rappaport EF, Grant SF, White PS, Hakonarson H.

Genome Res. 2009 Sep;19(9):1682-90. Epub 2009 Jul 10.PMID: 19592680 [PubMed - in process]Related articles

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

Zhao J, Li M, Bradfield JP, Wang K, Zhang H, Sleiman P, Kim CE, Annaiah K, Glaberson W, Glessner JT, Otieno FG, Thomas KA, Garris M, Hou C, Frackelton EC, Chiavacci RM, Berkowitz RI, Hakonarson H, Grant SF.

Diabetes. 2009 Oct;58(10):2414-8. Epub 2009 Jul 10.PMID: 19592620 [PubMed - indexed for MEDLINE]Related articles

Genome-wide association studies in type 1 diabetes, inflammatory bowel disease and other immune-mediated disorders.

Hakonarson H, Grant SF.

Semin Immunol. 2009 Jun 30. [Epub ahead of print]PMID: 19574059 [PubMed - as supplied by publisher]Related articles

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.

Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, Kustanovich V, Lajonchere CM, Singleton A, Kim J, Wassink TH, McMahon WM, Owley T, Sweeney JA, Coon H, Nurnberger JI, Li M, Cantor RM, Minshew NJ, Sutcliffe JS, Cook EH, Dawson G, Buxbaum JD, Grant SF, Schellenberg GD, Geschwind DH, Hakonarson H.

PLoS Genet. 2009 Jun;5(6):e1000536. Epub 2009 Jun 26.PMID: 19557195 [PubMed - indexed for MEDLINE]Related articlesFree article

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.

Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'arcy M, Deberardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, Grant SF, Berrettini W, Devoto M, Shaikh TH, Hakonarson H, White PS.

Mol Psychiatry. 2009 Jun 23. [Epub ahead of print]PMID: 19546859 [PubMed - as supplied by publisher]Related articles

Copy number variation at 1q21.1 associated with neuroblastoma.

Diskin SJ, Hou C, Glessner JT, Attiyeh EF, Laudenslager M, Bosse K, Cole K, Mossé YP, Wood A, Lynch JE, Pecor K, Diamond M, Winter C, Wang K, Kim C, Geiger EA, McGrady PW, Blakemore AI, London WB, Shaikh TH, Bradfield J, Grant SF, Li H, Devoto M, Rappaport ER, Hakonarson H, Maris JM.

Nature. 2009 Jun 18;459(7249):987-91.PMID: 19536264 [PubMed - indexed for MEDLINE]Related articlesFree article

The Role of Obesity-associated Loci Identified in Genome-wide Association Studies in the Determination of Pediatric BMI.

Zhao J, Bradfield JP, Li M, Wang K, Zhang H, Kim CE, Annaiah K, Glessner JT, Thomas K, Garris M, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Chiavacci RM, Berkowitz RI, Hakonarson H, Grant SF.

Obesity (Silver Spring). 2009 Dec;17(12):2254-7. Epub 2009 May 28.PMID: 19478790 [PubMed - in process]Related articles

Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies.

Qu HQ, Grant SF, Bradfield JP, Kim C, Frackelton E, Hakonarson H, Polychronakos C.

J Med Genet. 2009 Aug;46(8):553-4. Epub 2009 May 21.PMID: 19465406 [PubMed - indexed for MEDLINE]Related articles

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.

Capasso M, Devoto M, Hou C, Asgharzadeh S, Glessner JT, Attiyeh EF, Mosse YP, Kim C, Diskin SJ, Cole KA, Bosse K, Diamond M, Laudenslager M, Winter C, Bradfield JP, Scott RH, Jagannathan J, Garris M, McConville C, London WB, Seeger RC, Grant SF, Li H, Rahman N, Rappaport E, Hakonarson H, Maris JM.

Nat Genet. 2009 Jun;41(6):718-723. Epub 2009 May 3.PMID: 19412175 [PubMed - as supplied by publisher]Related articles

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):569-73. Epub 2009 Apr 28.PMID: 19404257 [PubMed - indexed for MEDLINE]Related articles

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):528-33. Epub 2009 Apr 28.PMID: 19404256 [PubMed - indexed for MEDLINE]Related articles

Genome-wide association studies in type 1 diabetes.

Grant SF, Hakonarson H.

Curr Diab Rep. 2009 Apr;9(2):157-63. Review.PMID: 19323961 [PubMed - indexed for MEDLINE]Related articles

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry.

Grant SF, Bradfield JP, Zhang H, Wang K, Kim CE, Annaiah K, Santa E, Glessner JT, Thomas K, Garris M, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Imielinski M, Chiavacci RM, Li M, Berkowitz RI, Hakonarson H.

Obesity (Silver Spring). 2009 Jul;17(7):1461-5. Epub 2009 Mar 5.PMID: 19265794 [PubMed - indexed for MEDLINE]Related articles

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease.

Wang K, Zhang H, Kugathasan S, Annese V, Bradfield JP, Russell RK, Sleiman PM, Imielinski M, Glessner J, Hou C, Wilson DC, Walters T, Kim C, Frackelton EC, Lionetti P, Barabino A, Van Limbergen J, Guthery S, Denson L, Piccoli D, Li M, Dubinsky M, Silverberg M, Griffiths A, Grant SF, Satsangi J, Baldassano R, Hakonarson H.

Am J Hum Genet. 2009 Mar;84(3):399-405. Epub 2009 Feb 26.PMID: 19249008 [PubMed - indexed for MEDLINE]Related articlesFree article

ATOM: a powerful gene-based association test by combining optimally weighted markers.

Li M, Wang K, Grant SF, Hakonarson H, Li C.

Bioinformatics. 2009 Feb 15;25(4):497-503. Epub 2008 Dec 15.PMID: 19074959 [PubMed - indexed for MEDLINE]Related articles

SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.

Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB.

Hum Mutat. 2009 Mar;30(3):371-8.PMID: 19058200 [PubMed - indexed for MEDLINE]Related articles

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.

Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, Li M, Derohannessian S, de Bakker PI, Bailey SD, Montpetit A, Edmondson AC, Taylor K, Gai X, Wang SS, Fornage M, Shaikh T, Groop L, Boehnke M, Hall AS, Hattersley AT, Frackelton E, Patterson N, Chiang CW, Kim CE, Fabsitz RR, Ouwehand W, Price AL, Munroe P, Caulfield M, Drake T, Boerwinkle E, Reich D, Whitehead AS, Cappola TP, Samani NJ, Lusis AJ, Schadt E, Wilson JG, Koenig W, McCarthy MI, Kathiresan S, Gabriel SB, Hakonarson H, Anand SS, Reilly M, Engert JC, Nickerson DA, Rader DJ, Hirschhorn JN, Fitzgerald GA.

PLoS One. 2008;3(10):e3583. Epub 2008 Oct 31.PMID: 18974833 [PubMed - indexed for MEDLINE]Related articlesFree article

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.

Grant SF, Qu HQ, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Taback SP, Frackelton EC, Eckert AW, Annaiah K, Lawson ML, Otieno FG, Santa E, Shaner JL, Smith RM, Skraban R, Imielinski M, Chiavacci RM, Grundmeier RW, Stanley CA, Kirsch SE, Waggott D, Paterson AD, Monos DS; DCCT/EDIC Research Group, Polychronakos C, Hakonarson H.

Diabetes. 2009 Jan;58(1):290-5. Epub 2008 Oct 7.PMID: 18840781 [PubMed - indexed for MEDLINE]Related articlesFree article

Modeling genetic inheritance of copy number variations.

Wang K, Chen Z, Tadesse MG, Glessner J, Grant SF, Hakonarson H, Bucan M, Li M.

Nucleic Acids Res. 2008 Dec;36(21):e138. Epub 2008 Oct 2.PMID: 18832372 [PubMed - indexed for MEDLINE]Related articlesFree article

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

Sleiman PM, Annaiah K, Imielinski M, Bradfield JP, Kim CE, Frackelton EC, Glessner JT, Eckert AW, Otieno FG, Santa E, Thomas K, Smith RM, Glaberson W, Garris M, Gunnlaugsson S, Chiavacci RM, Allen J, Spergel J, Grundmeier R, Grunstein MM, Magnusson M, Bisgaard H, Grant SF, Hakonarson H.

J Allergy Clin Immunol. 2008 Dec;122(6):1225-7. Epub 2008 Aug 28. No abstract available. PMID: 18760456 [PubMed - indexed for MEDLINE]Related articles

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.

Kugathasan S, Baldassano RN, Bradfield JP, Sleiman PM, Imielinski M, Guthery SL, Cucchiara S, Kim CE, Frackelton EC, Annaiah K, Glessner JT, Santa E, Willson T, Eckert AW, Bonkowski E, Shaner JL, Smith RM, Otieno FG, Peterson N, Abrams DJ, Chiavacci RM, Grundmeier R, Mamula P, Tomer G, Piccoli DA, Monos DS, Annese V, Denson LA, Grant SF, Hakonarson H.

Nat Genet. 2008 Oct;40(10):1211-5. Epub 2008 Aug 31.PMID: 18758464 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.

Behrens EM, Finkel TH, Bradfield JP, Kim CE, Linton L, Casalunovo T, Frackelton EC, Santa E, Otieno FG, Glessner JT, Chiavacci RM, Grant SF, Hakonarson H.

Arthritis Rheum. 2008 Jul;58(7):2206-7. No abstract available. PMID: 18576341 [PubMed - indexed for MEDLINE]Related articlesFree article

Microarray technology and applications in the arena of genome-wide association.

Grant SF, Hakonarson H.

Clin Chem. 2008 Jul;54(7):1116-24. Epub 2008 May 22. Review.PMID: 18499899 [PubMed - indexed for MEDLINE]Related articlesFree article

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

Maris JM, Mosse YP, Bradfield JP, Hou C, Monni S, Scott RH, Asgharzadeh S, Attiyeh EF, Diskin SJ, Laudenslager M, Winter C, Cole KA, Glessner JT, Kim C, Frackelton EC, Casalunovo T, Eckert AW, Capasso M, Rappaport EF, McConville C, London WB, Seeger RC, Rahman N, Devoto M, Grant SF, Li H, Hakonarson H.

N Engl J Med. 2008 Jun 12;358(24):2585-93. Epub 2008 May 7.PMID: 18463370 [PubMed - indexed for MEDLINE]Related articlesFree article

Association analysis of type 2 diabetes Loci in type 1 diabetes.

Qu HQ, Grant SF, Bradfield JP, Kim C, Frackelton E, Hakonarson H, Polychronakos C.

Diabetes. 2008 Jul;57(7):1983-6. Epub 2008 Apr 21.PMID: 18426861 [PubMed - indexed for MEDLINE]Related articlesFree article

Classification of genetic profiles of Crohn's disease: a focus on the ATG16L1 gene.

Grant SF, Baldassano RN, Hakonarson H.

Expert Rev Mol Diagn. 2008 Mar;8(2):199-207. Review.PMID: 18366306 [PubMed - indexed for MEDLINE]Related articles

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

Grant SF, Li M, Bradfield JP, Kim CE, Annaiah K, Santa E, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Imielinski M, Eckert AW, Chiavacci RM, Berkowitz RI, Hakonarson H.

PLoS One. 2008 Mar 12;3(3):e1746.PMID: 18335027 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study.

Hakonarson H, Qu HQ, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Casalunovo T, Taback SP, Frackelton EC, Eckert AW, Annaiah K, Lawson ML, Otieno FG, Santa E, Shaner JL, Smith RM, Onyiah CC, Skraban R, Chiavacci RM, Robinson LJ, Stanley CA, Kirsch SE, Devoto M, Monos DS, Grant SF, Polychronakos C.

Diabetes. 2008 Apr;57(4):1143-6. Epub 2008 Jan 15.PMID: 18198356 [PubMed - indexed for MEDLINE]Related articlesFree article

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.

Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M.

Genome Res. 2007 Nov;17(11):1665-74. Epub 2007 Oct 5.PMID: 17921354 [PubMed - indexed for MEDLINE]Related articlesFree article

Intraoperative gamma imaging of axillary sentinel lymph nodes in breast cancer patients.

Aarsvod JN, Greene CM, Mintzer RA, Grant SF, Styblo TM, Alazraki NP, Patt BE, Caravaglia GM, Li J, Iwanczyk JS.

Phys Med. 2006;21 Suppl 1:76-9.PMID: 17646000 [PubMed - in process]Related articles

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

Hakonarson H, Grant SF, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Casalunovo T, Taback SP, Frackelton EC, Lawson ML, Robinson LJ, Skraban R, Lu Y, Chiavacci RM, Stanley CA, Kirsch SE, Rappaport EF, Orange JS, Monos DS, Devoto M, Qu HQ, Polychronakos C.

Nature. 2007 Aug 2;448(7153):591-4. Epub 2007 Jul 15.PMID: 17632545 [PubMed - indexed for MEDLINE]Related articles

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease.

Baldassano RN, Bradfield JP, Monos DS, Kim CE, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Kanterakis S, Shaner JL, Smith RM, Eckert AW, Robinson LJ, Onyiah CC, Abrams DJ, Chiavacci RM, Skraban R, Devoto M, Grant SF, Hakonarson H.

Gut. 2007 Aug;56(8):1171-3. No abstract available. PMID: 17625155 [PubMed - indexed for MEDLINE]Related articles

Recent development in pharmacogenomics: from candidate genes to genome-wide association studies.

Grant SF, Hakonarson H.

Expert Rev Mol Diagn. 2007 Jul;7(4):371-93. Review.PMID: 17620046 [PubMed - indexed for MEDLINE]Related articles

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.

Baldassano RN, Bradfield JP, Monos DS, Kim CE, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Kanterakis S, Shaner JL, Smith RM, Eckert AW, Robinson LJ, Onyiah CC, Abrams DJ, Chiavacci RM, Skraban R, Devoto M, Grant SF, Hakonarson H.

Clin Gastroenterol Hepatol. 2007 Aug;5(8):972-6. Epub 2007 Jul 6.PMID: 17618837 [PubMed - indexed for MEDLINE]Related articles

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution.

Helgason A, Pálsson S, Thorleifsson G, Grant SF, Emilsson V, Gunnarsdottir S, Adeyemo A, Chen Y, Chen G, Reynisdottir I, Benediktsson R, Hinney A, Hansen T, Andersen G, Borch-Johnsen K, Jorgensen T, Schäfer H, Faruque M, Doumatey A, Zhou J, Wilensky RL, Reilly MP, Rader DJ, Bagger Y, Christiansen C, Sigurdsson G, Hebebrand J, Pedersen O, Thorsteinsdottir U, Gulcher JR, Kong A, Rotimi C, Stefánsson K.

Nat Genet. 2007 Feb;39(2):218-25. Epub 2007 Jan 7.PMID: 17206141 [PubMed - indexed for MEDLINE]Related articles

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.

Grant SF, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, Helgason A, Stefansson H, Emilsson V, Helgadottir A, Styrkarsdottir U, Magnusson KP, Walters GB, Palsdottir E, Jonsdottir T, Gudmundsdottir T, Gylfason A, Saemundsdottir J, Wilensky RL, Reilly MP, Rader DJ, Bagger Y, Christiansen C, Gudnason V, Sigurdsson G, Thorsteinsdottir U, Gulcher JR, Kong A, Stefansson K.

Nat Genet. 2006 Mar;38(3):320-3. Epub 2006 Jan 15.PMID: 16415884 [PubMed - indexed for MEDLINE]Related articles

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.

Helgadottir A, Manolescu A, Helgason A, Thorleifsson G, Thorsteinsdottir U, Gudbjartsson DF, Gretarsdottir S, Magnusson KP, Gudmundsson G, Hicks A, Jonsson T, Grant SF, Sainz J, O'Brien SJ, Sveinbjornsdottir S, Valdimarsson EM, Matthiasson SE, Levey AI, Abramson JL, Reilly MP, Vaccarino V, Wolfe ML, Gudnason V, Quyyumi AA, Topol EJ, Rader DJ, Thorgeirsson G, Gulcher JR, Hakonarson H, Kong A, Stefansson K.

Nat Genet. 2006 Jan;38(1):68-74. Epub 2005 Nov 10.PMID: 16282974 [PubMed - indexed for MEDLINE]Related articles

Contribution of the collagen I alpha1 and vitamin D receptor genes to the risk of hip fracture in elderly women.

Nguyen TV, Esteban LM, White CP, Grant SF, Center JR, Gardiner EM, Eisman JA.

J Clin Endocrinol Metab. 2005 Dec;90(12):6575-9. Epub 2005 Sep 13.PMID: 16159929 [PubMed - indexed for MEDLINE]Related articlesFree article

Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population.

Helgadottir A, Gretarsdottir S, St Clair D, Manolescu A, Cheung J, Thorleifsson G, Pasdar A, Grant SF, Whalley LJ, Hakonarson H, Thorsteinsdottir U, Kong A, Gulcher J, Stefansson K, MacLeod MJ.

Am J Hum Genet. 2005 Mar;76(3):505-9. Epub 2005 Jan 7.PMID: 15640973 [PubMed - indexed for MEDLINE]Related articlesFree article

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.

Helgadottir A, Manolescu A, Thorleifsson G, Gretarsdottir S, Jonsdottir H, Thorsteinsdottir U, Samani NJ, Gudmundsson G, Grant SF, Thorgeirsson G, Sveinbjornsdottir S, Valdimarsson EM, Matthiasson SE, Johannsson H, Gudmundsdottir O, Gurney ME, Sainz J, Thorhallsdottir M, Andresdottir M, Frigge ML, Topol EJ, Kong A, Gudnason V, Hakonarson H, Gulcher JR, Stefansson K.

Nat Genet. 2004 Mar;36(3):233-9. Epub 2004 Feb 8.PMID: 14770184 [PubMed - indexed for MEDLINE]Related articles

Linkage of osteoporosis to chromosome 20p12 and association to BMP2.

Styrkarsdottir U, Cazier JB, Kong A, Rolfsson O, Larsen H, Bjarnadottir E, Johannsdottir VD, Sigurdardottir MS, Bagger Y, Christiansen C, Reynisdottir I, Grant SF, Jonasson K, Frigge ML, Gulcher JR, Sigurdsson G, Stefansson K.

PLoS Biol. 2003 Dec;1(3):E69. Epub 2003 Nov 3.PMID: 14691541 [PubMed - indexed for MEDLINE]Related articlesFree article

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

Reynisdottir I, Thorleifsson G, Benediktsson R, Sigurdsson G, Emilsson V, Einarsdottir AS, Hjorleifsdottir EE, Orlygsdottir GT, Bjornsdottir GT, Saemundsdottir J, Halldorsson S, Hrafnkelsdottir S, Sigurjonsdottir SB, Steinsdottir S, Martin M, Kochan JP, Rhees BK, Grant SF, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR.

Am J Hum Genet. 2003 Aug;73(2):323-35. Epub 2003 Jul 8.PMID: 12851856 [PubMed - indexed for MEDLINE]Related articlesFree article

Immunohistochemical evaluation of sentinel lymph nodes in breast carcinoma patients.

Cohen C, Alazraki N, Styblo T, Waldrop SM, Grant SF, Larsen T.

Appl Immunohistochem Mol Morphol. 2002 Dec;10(4):296-303.PMID: 12607596 [PubMed - indexed for MEDLINE]Related articles

SNP genotyping on a genome-wide amplified DOP-PCR template.

Grant SF, Steinlicht S, Nentwich U, Kern R, Burwinkel B, Tolle R.

Nucleic Acids Res. 2002 Nov 15;30(22):e125.PMID: 12434007 [PubMed - indexed for MEDLINE]Related articlesFree article

The inheritance of rheumatoid arthritis in Iceland.

Grant SF, Thorleifsson G, Frigge ML, Thorsteinsson J, Gunnlaugsdóttir B, Geirsson AJ, Gudmundsson M, Vikingsson A, Erlendsson K, Valsson J, Jónsson H, Gudbjartsson DF, Stefánsson K, Gulcher JR, Steinsson K.

Arthritis Rheum. 2001 Oct;44(10):2247-54.PMID: 11665965 [PubMed - indexed for MEDLINE]Related articles