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

161.

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
162.

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
163.

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
164.

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
165.

Elastic fiber homeostasis requires lysyl oxidase-like 1 protein.

Nat. Genet.
Liu X, Zhao Y, Gao J, Pawlyk B, Starcher B, Spencer JA, Yanagisawa H, Zuo J, Li T.
| 01 25, 2004
166.

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Nat. Genet.
Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA.
| 11 30, 2003
167.

Cryptic boundaries in roof plate and choroid plexus identified by intersectional gene activation.

Nat. Genet.
Awatramani R, Soriano P, Rodriguez C, Mai JJ, Dymecki SM.
| 08 17, 2003
168.

C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression.

Nat. Genet.
Reboul J, Vaglio P, Rual JF, Lamesch P, Martinez M, Armstrong CM, Li S, Jacotot L, Bertin N, Janky R, Moore T, Hudson JR, Hartley JL, Brasch MA, Vandenhaute J, Boulton S, Endress GA, Jenna S, Chevet E, Papasotiropoulos V, Tolias PP, Ptacek J, Snyder M, Huang R, Chance MR, Lee H, Doucette-Stamm L, Hill DE, Vidal M.
| 4 8, 2003
170.

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.

Nat. Genet.
Nauli SM, Alenghat FJ, Luo Y, Williams E, Vassilev P, Li X, Elia AE, Lu W, Brown EM, Quinn SJ, Ingber DE, Zhou J.
| 01 06, 2003
171.

A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevity.

Nat. Genet.
Lee SS, Lee RY, Fraser AG, Kamath RS, Ahringer J, Ruvkun G.
| 11 25, 2002
174.

beta-cell-specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter beta-cell mass.

Nat. Genet.
Kulkarni RN, Holzenberger M, Shih DQ, Ozcan U, Stoffel M, Magnuson MA, Kahn CR.
| 04 01, 2002
175.

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.

Nat. Genet.
Herron BJ, Lu W, Rao C, Liu S, Peters H, Bronson RT, Justice MJ, McDonald JD, Beier DR.
| 01 02, 2002
176.

Identification of foreign gene sequences by transcript filtering against the human genome.

Nat. Genet.
Weber G, Shendure J, Tanenbaum DM, Church GM, Meyerson M.
| 01 14, 2002
177.

Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin.

Nat. Genet.
Xu X, Meiler SE, Zhong TP, Mohideen M, Crossley DA, Burggren WW, Fishman MC.
| 01 14, 2002
178.

MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia.

Nat. Genet.
Armstrong SA, Staunton JE, Silverman LB, Pieters R, den Boer ML, Minden MD, Sallan SE, Lander ES, Golub TR, Korsmeyer SJ.
| 12 03, 2001
179.

Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae.

Nat. Genet.
Ge H, Liu Z, Church GM, Vidal M.
| 11 6, 2001
180.

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Nat. Genet.
Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC.
| 10 16, 2001