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

101.

Variation in complement factor 3 is associated with risk of age-related macular degeneration.

Nat. Genet.
Maller JB, Fagerness JA, Reynolds RC, Neale BM, Daly MJ, Seddon JM.
| 09 02, 2007
102.

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.

Nat. Genet.
Kantarci S, Al-Gazali L, Hill RS, Donnai D, Black GC, Bieth E, Chassaing N, Lacombe D, Devriendt K, Teebi A, Loscertales M, Robson C, Liu T, MacLaughlin DT, Noonan KM, Russell MK, Walsh CA, Donahoe PK, Pober BR.
| 07 15, 2007
103.

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.

Nat. Genet.
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, Wacholder S, Wang Z, Welch R, Hutchinson A, Wang J, Yu K, Chatterjee N, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF, Hoover RN, Thomas G, Chanock SJ.
| 05 27, 2007
104.

High-throughput oncogene mutation profiling in human cancer.

Nat. Genet.
Thomas RK, Baker AC, Debiasi RM, Winckler W, Laframboise T, Lin WM, Wang M, Feng W, Zander T, MacConaill L, Macconnaill LE, Lee JC, Nicoletti R, Hatton C, Goyette M, Girard L, Majmudar K, Ziaugra L, Wong KK, Gabriel S, Beroukhim R, Peyton M, Barretina J, Dutt A, Emery C, Greulich H, Shah K, Sasaki H, Gazdar A, Minna J, Armstrong SA, Mellinghoff IK, Hodi FS, Dranoff G, Mischel PS, Cloughesy TF, Nelson SF, Liau LM, Mertz K, Rubin MA, Moch H, Loda M, Catalona W, Fletcher J, Signoretti S, Kaye F, Anderson KC, Demetri GD, Dummer R, Wagner S, Herlyn M, Sellers WR, Meyerson M, Garraway LA.
| 02 11, 2007
105.

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.

Nat. Genet.
Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP.
| 12 31, 2006
106.

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.

Nat. Genet.
Bertram L, McQueen MB, Mullin K, Blacker D, Tanzi RE.
| 12 29, 2006
107.

Germline gain-of-function mutations in SOS1 cause Noonan syndrome.

Nat. Genet.
Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS.
| 12 03, 2006
108.

BMP2 activity, although dispensable for bone formation, is required for the initiation of fracture healing.

Nat. Genet.
Tsuji K, Bandyopadhyay A, Harfe BD, Cox K, Kakar S, Gerstenfeld L, Einhorn T, Tabin CJ, Rosen V.
| 11 12, 2006
109.

Essential role of Jun family transcription factors in PU.1 knockdown-induced leukemic stem cells.

Nat. Genet.
Steidl U, Rosenbauer F, Verhaak RG, Gu X, Ebralidze A, Otu HH, Klippel S, Steidl C, Bruns I, Costa DB, Wagner K, Aivado M, Kobbe G, Valk PJ, Passegué E, Libermann TA, Delwel R, Tenen DG.
| 10 15, 2006
110.

Genome-wide analysis of estrogen receptor binding sites.

Nat. Genet.
Carroll JS, Meyer CA, Song J, Li W, Geistlinger TR, Eeckhoute J, Brodsky AS, Keeton EK, Fertuck KC, Hall GF, Wang Q, Bekiranov S, Sementchenko V, Fox EA, Silver PA, Gingeras TR, Liu XS, Brown M.
| 10 01, 2006
112.

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.

Nat. Genet.
Maller J, George S, Purcell S, Fagerness J, Altshuler D, Daly MJ, Seddon JM.
| 08 27, 2006
113.

A signature of chromosomal instability inferred from gene expression profiles predicts clinical outcome in multiple human cancers.

Nat. Genet.
Carter SL, Eklund AC, Kohane IS, Harris LN, Szallasi Z.
| 08 20, 2006
114.

Principal components analysis corrects for stratification in genome-wide association studies.

Nat. Genet.
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D.
| 07 23, 2006
115.

Evaluating and improving power in whole-genome association studies using fixed marker sets.

Nat. Genet.
Pe'er I, de Bakker PI, Maller J, Yelensky R, Altshuler D, Daly MJ.
| 05 21, 2006
116.

Total insulin and IGF-I resistance in pancreatic beta cells causes overt diabetes.

Nat. Genet.
Ueki K, Okada T, Hu J, Liew CW, Assmann A, Dahlgren GM, Peters JL, Shackman JG, Zhang M, Artner I, Satin LS, Stein R, Holzenberger M, Kennedy RT, Kahn CR, Kulkarni RN.
| 04 23, 2006
117.

Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression.

Nat. Genet.
Babitt JL, Huang FW, Wrighting DM, Xia Y, Sidis Y, Samad TA, Campagna JA, Chung RT, Schneyer AL, Woolf CJ, Andrews NC, Lin HY.
| 04 09, 2006
118.

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.

Nat. Genet.
Kraytsberg Y, Kudryavtseva E, McKee AC, Geula C, Kowall NW, Khrapko K.
| 04 09, 2006
119.

Long-range polony haplotyping of individual human chromosome molecules.

Nat. Genet.
Zhang K, Zhu J, Shendure J, Porreca GJ, Aach JD, Mitra RD, Church GM.
| 02 19, 2006
120.

Common deletion polymorphisms in the human genome.

Nat. Genet.
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM.
| 2 10, 2006