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.

PU.1 is a major downstream target of AML1 (RUNX1) in adult mouse hematopoiesis.

Nat. Genet.
Huang G, Zhang P, Hirai H, Elf S, Yan X, Chen Z, Koschmieder S, Okuno Y, Dayaram T, Growney JD, Shivdasani RA, Gilliland DG, Speck NA, Nimer SD, Tenen DG.
| 11 11, 2007
102.

Evidence that homologous X-chromosome pairing requires transcription and Ctcf protein.

Nat. Genet.
Xu N, Donohoe ME, Silva SS, Lee JT.
| 10 21, 2007
103.

Network modeling links breast cancer susceptibility and centrosome dysfunction.

Nat. Genet.
Pujana MA, Han JD, Starita LM, Stevens KN, Tewari M, Ahn JS, Rennert G, Moreno V, Kirchhoff T, Gold B, Assmann V, Elshamy WM, Rual JF, Levine D, Rozek LS, Gelman RS, Gunsalus KC, Greenberg RA, Sobhian B, Bertin N, Venkatesan K, Ayivi-Guedehoussou N, Solé X, Hernández P, Lázaro C, Nathanson KL, Weber BL, Cusick ME, Hill DE, Offit K, Livingston DM, Gruber SB, Parvin JD, Vidal M.
| 10 07, 2007
105.

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Nat. Genet.
Lee C, Iafrate AJ, Brothman AR.
| 9 5, 2007
106.

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
107.

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
108.

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
109.

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
110.

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
111.

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
112.

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
113.

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
114.

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
115.

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
117.

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
118.

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
119.

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
120.

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