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.

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.

Nat. Genet.
Allen NC, Bagade S, McQueen MB, Ioannidis JP, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L.
| 6 28, 2008
102.

Exposing the fitness contribution of duplicated genes.

Nat. Genet.
DeLuna A, Vetsigian K, Shoresh N, Hegreness M, Colón-González M, Chao S, Kishony R.
| 04 13, 2008
103.

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA).

Nat. Genet.
Finberg KE, Heeney MM, Campagna DR, Aydinok Y, Pearson HA, Hartman KR, Mayo MM, Samuel SM, Strouse JJ, Markianos K, Andrews NC, Fleming MD.
| 04 13, 2008
104.

THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia.

Nat. Genet.
Tran PV, Haycraft CJ, Besschetnova TY, Turbe-Doan A, Stottmann RW, Herron BJ, Chesebro AL, Qiu H, Scherz PJ, Shah JV, Yoder BK, Beier DR.
| 03 09, 2008
105.

Exploiting position effects and the gypsy retrovirus insulator to engineer precisely expressed transgenes.

Nat. Genet.
Markstein M, Pitsouli C, Villalta C, Celniker SE, Perrimon N.
| 03 02, 2008
106.

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

Nat. Genet.
Kathiresan S, Melander O, Guiducci C, Surti A, Burtt NP, Rieder MJ, Cooper GM, Roos C, Voight BF, Havulinna AS, Wahlstrand B, Hedner T, Corella D, Tai ES, Ordovas JM, Berglund G, Vartiainen E, Jousilahti P, Hedblad B, Taskinen MR, Newton-Cheh C, Salomaa V, Peltonen L, Groop L, Altshuler DM, Orho-Melander M.
| 01 13, 2008
107.

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
108.

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

Nat. Genet.
Xu N, Donohoe ME, Silva SS, Lee JT.
| 10 21, 2007
109.

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
111.

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Nat. Genet.
Lee C, Iafrate AJ, Brothman AR.
| 9 5, 2007
112.

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
113.

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
114.

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
115.

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
116.

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
117.

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
118.

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
119.

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
120.

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