Paper Chase is a research database designed to offer abstracts of research articles published in journals that have a highly rated impact factor as determined by ISI Impact Factor and PageRank. Abstracts are organized by date, with the most recently published papers listed first. 

Paper Chase

141.

A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility.

Nat. Genet.
Reich D, Patterson N, De Jager PL, McDonald GJ, Waliszewska A, Tandon A, Lincoln RR, DeLoa C, Fruhan SA, Cabre P, Bera O, Semana G, Kelly MA, Francis DA, Ardlie K, Khan O, Cree BA, Hauser SL, Oksenberg JR, Hafler DA.
| 09 25, 2005
142.

Distinct epigenetic changes in the stromal cells of breast cancers.

Nat. Genet.
Hu M, Yao J, Cai L, Bachman KE, van den Brûle F, Velculescu V, Polyak K.
| 07 10, 2005
143.

TACI is mutant in common variable immunodeficiency and IgA deficiency.

Nat. Genet.
Castigli E, Wilson SA, Garibyan L, Rachid R, Bonilla F, Schneider L, Geha RS.
| 07 10, 2005
144.

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function.

Nat. Genet.
Reiser J, Polu KR, Möller CC, Kenlan P, Altintas MM, Wei C, Faul C, Herbert S, Villegas I, Avila-Casado C, McGee M, Sugimoto H, Brown D, Kalluri R, Mundel P, Smith PL, Clapham DE, Pollak MR.
| 05 27, 2005
145.

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

Nat. Genet.
Schönberger J, Wang L, Shin JT, Kim SD, Depreux FF, Zhu H, Zon L, Pizard A, Kim JB, Macrae CA, Mungall AJ, Seidman JG, Seidman CE.
| 02 27, 2005
147.

Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib.

Nat. Genet.
Bastepe M, Fröhlich LF, Linglart A, Abu-Zahra HS, Tojo K, Ward LM, Jüppner H.
| 12 12, 2004
148.

Modular epistasis in yeast metabolism.

Nat. Genet.
Segrè D, Deluna A, Church GM, Kishony R.
| 12 12, 2004
149.

Rapid analysis of the DNA-binding specificities of transcription factors with DNA microarrays.

Nat. Genet.
Mukherjee S, Berger MF, Jona G, Wang XS, Muzzey D, Snyder M, Young RA, Bulyk ML.
| 11 14, 2004
150.

Targeted gene alteration in Caenorhabditis elegans by gene conversion.

Nat. Genet.
Barrett PL, Fleming JT, Göbel V.
| 10 24, 2004
151.

MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression.

Nat. Genet.
Mansfield JH, Harfe BD, Nissen R, Obenauer J, Srineel J, Chaudhuri A, Farzan-Kashani R, Zuker M, Pasquinelli AE, Ruvkun G, Sharp PA, Tabin CJ, McManus MT.
| 09 12, 2004
152.

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Nat. Genet.
Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA.
| 08 22, 2004
153.

Detection of large-scale variation in the human genome.

Nat. Genet.
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C.
| 08 01, 2004
154.

Lymphatic reprogramming of blood vascular endothelium by Kaposi sarcoma-associated herpesvirus.

Nat. Genet.
Hong YK, Foreman K, Shin JW, Hirakawa S, Curry CL, Sage DR, Libermann T, Dezube BJ, Fingeroth JD, Detmar M.
| 06 27, 2004
155.

SUMO modification is required for in vivo Hox gene regulation by the Caenorhabditis elegans Polycomb group protein SOP-2.

Nat. Genet.
Zhang H, Smolen GA, Palmer R, Christoforou A, van den Heuvel S, Haber DA.
| 04 11, 2004
156.

An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in mice.

Nat. Genet.
Roy CN, Custodio AO, de Graaf J, Schneider S, Akpan I, Montross LK, Sanchez M, Gaudino A, Hentze MW, Andrews NC, Muckenthaler MU.
| 04 18, 2004
157.

Assessing the impact of population stratification on genetic association studies.

Nat. Genet.
Freedman ML, Reich D, Penney KL, McDonald GJ, Mignault AA, Patterson N, Gabriel SB, Topol EJ, Smoller JW, Pato CN, Pato MT, Petryshen TL, Kolonel LN, Lander ES, Sklar P, Henderson B, Hirschhorn JN, Altshuler D.
| 03 28, 2004
158.

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Nat. Genet.
Watts GD, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, Pestronk A, Whyte MP, Kimonis VE.
| 03 21, 2004
159.

Gene expression-based high-throughput screening(GE-HTS) and application to leukemia differentiation.

Nat. Genet.
Stegmaier K, Ross KN, Colavito SA, O'Malley S, Stockwell BR, Golub TR.
| 02 08, 2004
160.

The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fate.

Nat. Genet.
Chae TH, Kim S, Marz KE, Hanson PI, Walsh CA.
| 02 01, 2004