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

1.

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.

Nat. Genet.
Robinson EB, St Pourcain B, Anttila V, Kosmicki JA, Bulik-Sullivan B, Grove J, Maller J, Samocha KE, Sanders SJ, Ripke S, Martin J, Hollegaard MV, Werge T, Hougaard DM, Neale BM, Evans DM, Skuse D, Mortensen PB, Børglum AD, Ronald A, Smith GD, Daly MJ.
| 03 21, 2016
2.

Screening for Autism Spectrum Disorder in Young Children: US Preventive Services Task Force Recommendation Statement.

JAMA.
Siu AL, Bibbins-Domingo K, Grossman DC, Baumann LC, Davidson KW, Ebell M, García FA, Gillman M, Herzstein J, Kemper AR, Krist AH, Kurth AE, Owens DK, Phillips WR, Phipps MG, Pignone MP.
| Feb 16, 2016
3.

Compromising the phosphodependent regulation of the GABAAR β3 subunit reproduces the core phenotypes of autism spectrum disorders.

Proc. Natl. Acad. Sci. U.S.A.
Vien TN, Modgil A, Abramian AM, Jurd R, Walker J, Brandon NJ, Terunuma M, Rudolph U, Maguire J, Davies PA, Moss SJ.
| Dec 1, 2015
5.

Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism.

Proc. Natl. Acad. Sci. U.S.A.
Prusiner SB, Woerman AL, Mordes DA, Watts JC, Rampersaud R, Berry DB, Patel S, Oehler A, Lowe JK, Kravitz SN, Geschwind DH, Glidden DV, Halliday GM, Middleton LT, Gentleman SM, Grinberg LT, Giles K.
| Sep 22, 2015
6.

Loss of δ-catenin function in severe autism.

Nature.
Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, Cheung SW, Martin CL, State MW, Talkowski ME, Cook E, Huganir R, Katsanis N, Chakravarti A.
| Apr 2, 2015
7.

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.

Nature.
Gabel HW, Kinde B, Stroud H, Gilbert CS, Harmin DA, Kastan NR, Hemberg M, Ebert DH, Greenberg ME.
| Jun 4, 2015
8.

New human-specific brain landmark: the depth asymmetry of superior temporal sulcus.

Proc. Natl. Acad. Sci. U.S.A.
Leroy F, Cai Q, Bogart SL, Dubois J, Coulon O, Monzalvo K, Fischer C, Glasel H, Van der Haegen L, Bénézit A, Lin CP, Kennedy DN, Ihara AS, Hertz-Pannier L, Moutard ML, Poupon C, Brysbaert M, Roberts N, Hopkins WD, Mangin JF, Dehaene-Lambertz G.
| Jan 27, 2015
9.

Monoallelic expression of the human FOXP2 speech gene.

Proc. Natl. Acad. Sci. U.S.A.
Adegbola AA, Cox GF, Bradshaw EM, Hafler DA, Gimelbrant A, Chess A.
| Jun 2, 2015
10.

Sulforaphane treatment of autism spectrum disorder (ASD).

Proc. Natl. Acad. Sci. U.S.A.
Singh K, Connors SL, Macklin EA, Smith KD, Fahey JW, Talalay P, Zimmerman AW.
| Oct 28, 2014
11.

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.

Proc. Natl. Acad. Sci. U.S.A.
Sugathan A, Biagioli M, Golzio C, Erdin S, Blumenthal I, Manavalan P, Ragavendran A, Brand H, Lucente D, Miles J, Sheridan SD, Stortchevoi A, Kellis M, Haggarty SJ, Katsanis N, Gusella JF, Talkowski ME.
| Oct 21, 2014
12.

Autism as a disorder of prediction.

Proc. Natl. Acad. Sci. U.S.A.
Sinha P, Kjelgaard MM, Gandhi TK, Tsourides K, Cardinaux AL, Pantazis D, Diamond SP, Held RM.
| Oct 21, 2014
13.

Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.

Proc. Natl. Acad. Sci. U.S.A.
Robinson EB, Samocha KE, Kosmicki JA, McGrath L, Neale BM, Perlis RH, Daly MJ.
| Oct 21, 2014
14.

A framework for the interpretation of de novo mutation in human disease.

Nat. Genet.
Samocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A, Wall DP, MacArthur DG, Gabriel SB, DePristo M, Purcell SM, Palotie A, Boerwinkle E, Buxbaum JD, Cook EH, Gibbs RA, Schellenberg GD, Sutcliffe JS, Devlin B, Roeder K, Neale BM, Daly MJ.
| 08 03, 2014
15.

Most genetic risk for autism resides with common variation.

Nat. Genet.
Gaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reichert J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, Hultman CM, Devlin B, Roeder K, Buxbaum JD.
| 07 20, 2014
16.

Guidelines for investigating causality of sequence variants in human disease.

Nature.
MacArthur DG, Manolio TA, Dimmock DP, Rehm HL, Shendure J, Abecasis GR, Adams DR, Altman RB, Antonarakis SE, Ashley EA, Barrett JC, Biesecker LG, Conrad DF, Cooper GM, Cox NJ, Daly MJ, Gerstein MB, Goldstein DB, Hirschhorn JN, Leal SM, Pennacchio LA, Stamatoyannopoulos JA, Sunyaev SR, Valle D, Voight BF, Winckler W, Gunter C.
| Apr 24, 2014
17.

A polygenic burden of rare disruptive mutations in schizophrenia.

Nature.
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O'Dushlaine C, Chambert K, Bergen SE, Kähler A, Duncan L, Stahl E, Genovese G, Fernández E, Collins MO, Komiyama NH, Choudhary JS, Magnusson PK, Banks E, Shakir K, Garimella K, Fennell T, DePristo M, Grant SG, Haggarty SJ, Gabriel S, Scolnick EM, Lander ES, Hultman CM, Sullivan PF, McCarroll SA, Sklar P.
| Feb 13, 2014
18.

De novo mutations in schizophrenia implicate synaptic networks.

Nature.
Fromer M, Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S, Gormley P, Georgieva L, Rees E, Palta P, Ruderfer DM, Carrera N, Humphreys I, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Grant SG, Hannon E, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Kirov G, Palotie A, McCarroll SA, Holmans P, Sklar P, Owen MJ, Purcell SM, O'Donovan MC.
| Feb 13, 2014
19.

Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR.

Nature.
Ebert DH, Gabel HW, Robinson ND, Kastan NR, Hu LS, Cohen S, Navarro AJ, Lyst MJ, Ekiert R, Bird AP, Greenberg ME.
| Jul 18, 2013
20.

Examining and interpreting the female protective effect against autistic behavior.

Proc. Natl. Acad. Sci. U.S.A.
Robinson EB, Lichtenstein P, Anckarsäter H, Happé F, Ronald A.
| Mar 26, 2013