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Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.

Silverman EK, Mosley JD, Palmer LJ, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, Weiss ST.

Hum Mol Genet. 2002 Mar 15;11(6):623-32.


Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease.

Silverman EK, Palmer LJ, Mosley JD, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, Weiss ST.

Am J Hum Genet. 2002 May;70(5):1229-39. Epub 2002 Mar 25.


Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease.

Palmer LJ, Celedón JC, Chapman HA, Speizer FE, Weiss ST, Silverman EK.

Hum Mol Genet. 2003 May 15;12(10):1199-210. Erratum in: Hum Mol Genet. 2003 Aug 15;12(16):2085.


Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases.

Silverman EK, Mosley JD, Rao DC, Palmer LJ, Province MA, Elston RC, Weiss ST, Campbell EJ.

Hum Hered. 2001;52(4):223-32.


Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica.

Hersh CP, Soto-Quirós ME, Avila L, Lake SL, Liang C, Fournier E, Spesny M, Sylvia JS, Lazarus R, Hudson T, Verner A, Klanderman BJ, Freimer NB, Silverman EK, Celedón JC.

Thorax. 2007 Mar;62(3):224-30. Epub 2006 Nov 10.


Genome-wide linkage of forced mid-expiratory flow in chronic obstructive pulmonary disease.

DeMeo DL, Celedón JC, Lange C, Reilly JJ, Chapman HA, Sylvia JS, Speizer FE, Weiss ST, Silverman EK.

Am J Respir Crit Care Med. 2004 Dec 15;170(12):1294-301. Epub 2004 Sep 3.


Genetic linkage and association analysis of COPD-related traits on chromosome 8p.

Hersh CP, DeMeo DL, Raby BA, Litonjua AA, Sylvia JS, Sparrow D, Reilly JJ, Silverman EK.

COPD. 2006 Dec;3(4):189-94.


A genome-wide association study of pulmonary function measures in the Framingham Heart Study.

Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, Brandler BJ, Myers RH, Borecki IB, Silverman EK, Weiss ST, O'Connor GT.

PLoS Genet. 2009 Mar;5(3):e1000429. doi: 10.1371/journal.pgen.1000429. Epub 2009 Mar 20.


A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.

Hum Mol Genet. 2001 Nov 15;10(24):2751-65.


Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P.

Am J Hum Genet. 2000 Dec;67(6):1470-80. Epub 2000 Nov 6.


A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z.

Mol Vis. 2008 Apr 18;14:739-44.


Linkage genome scan for loci predisposing to panic disorder or agoraphobia.

Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.

Am J Med Genet. 2001 Aug 8;105(6):548-57.


A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E.

Am J Hum Genet. 2001 Jul;69(1):96-105. Epub 2001 May 25.


The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD).

Celedón JC, Lange C, Raby BA, Litonjua AA, Palmer LJ, DeMeo DL, Reilly JJ, Kwiatkowski DJ, Chapman HA, Laird N, Sylvia JS, Hernandez M, Speizer FE, Weiss ST, Silverman EK.

Hum Mol Genet. 2004 Aug 1;13(15):1649-56. Epub 2004 Jun 2.


Two-stage genome-wide linkage scan in keratoconus sib pair families.

Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, Yang H.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3791-5.


Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.

Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.

Arch Neurol. 2006 Nov;63(11):1591-8.


Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.

Celedón JC, Soto-Quiros ME, Avila L, Lake SL, Liang C, Fournier E, Spesny M, Hersh CP, Sylvia JS, Hudson TJ, Verner A, Klanderman BJ, Freimer NB, Silverman EK, Weiss ST.

Hum Genet. 2007 Jan;120(5):691-9. Epub 2006 Sep 26.


[Genetic features during chronic obstructive pulmonary disease].

Babusyte A, Sitkauskiene B, Sakalauskas R.

Medicina (Kaunas). 2006;42(7):527-35. Review. Lithuanian.


A genome-wide linkage scan for homocysteine levels suggests three regions of interest.

Vermeulen SH, van der Vleuten GM, de Graaf J, Hermus AR, Blom HJ, Stalenhoef AF, den Heijer M.

J Thromb Haemost. 2006 Jun;4(6):1303-7.


A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.

McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.

Mol Psychiatry. 2009 May;14(5):492-500. doi: 10.1038/ Epub 2008 Jan 29.

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