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2016
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.Legge, SE, Hamshere ML, Ripke S., Pardinas AF, Goldstein JI, Rees E., Richards AL, Leonenko G., Jorskog LF, Clozapine-Induced Agranulocytosis Consortium, Chambert KD, Collier DA, Genovese G., Giegling I., Holmans P., Jonasdottir A., Kirov G., McCarroll SA, MacCabe JH, Mantripragada K., et al. Molecular psychiatry, 2016/07/12, (2016) Read More / View Supplemental Materials
Abstract
Schizophrenia risk from complex variation of complement component 4.Sekar, A., Bialas AR, de Rivera H., Davis A., Hammond TR, Kamitaki N., Tooley K., Presumey J., Baum M., Van Doren V., Genovese G., Rose SA, Handsaker RE, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Daly M. J., Carroll MC, Stevens B., and McCarroll SA Nature, 2016/02/11, Volume 530, Issue 7589, p.177-83, (2016) Read More / View Supplemental Materials
Abstract
2015
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates.Palamara, PF, Francioli LC, Wilton PR, Genovese G., Gusev A., Finucane HK, Sankararaman S., Genome of the Netherlands Consortium, Sunyaev SR, de Bakker PI, Wakeley J., Pe'er I., and Price AL American journal of human genetics, 2015/11/11, (2015) Read More / View Supplemental Materials
Abstract
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.Vilhjálmsson, BJ, Yang J., Finucane HK, Gusev A., Lindström S., Ripke S., Genovese G., Loh PR, Bhatia G., Do R., Hayeck T., Won HH, and of in study Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery Biology Risk Inherited Variants Breast Cancer(DRIVE), Kathiresan S., Pato M., Pato C., Tamimi R., Stahl E., Zaitlen N., Pasaniuc B., et al. American journal of human genetics, 2015/10/01, Volume 97, Issue 4, p.576-92, (2015) Read More / View Supplemental Materials
Abstract
Dynamics of Tumor Heterogeneity Derived from Clonal Karyotypic Evolution.Laughney, AM, Elizalde S., Genovese G., and Bakhoum SF Cell reports, 2015/08/04, Volume 12, Issue 5, p.809-820, (2015) Read More / View Supplemental Materials
Abstract
Non-crossover gene conversions show strong GC bias and unexpected clustering in humans.Williams, AL, Genovese G., Dyer T., Altemose N., Truax K., Jun G., Patterson N., Myers SR, Curran JE, Duggirala R., Blangero J., Reich D., and Przeworski M. eLife, 2015/03/25, Volume 4, (2015) Read More / View Supplemental Materials
Abstract
Large multiallelic copy number variations in humans.Handsaker, RE, Van Doren V., Berman JR, Genovese G., Kashin S., Boettger LM, and McCarroll SA Nature genetics, 2015/01/26, (2015) Read More / View Supplemental Materials
Abstract
Copy number variation in bipolar disorder.Green, EK, Rees E., Walters JT, Smith KG, Forty L., Grozeva D., Moran JL, Sklar P., Ripke S., Chambert KD, Genovese G., McCarroll SA, Jones I., Jones L., Owen MJ, O'Donovan MC, Craddock N., and Kirov G. Molecular psychiatry, 2015/01/06, (2015) Read More / View Supplemental Materials
Abstract
Copy Number Variation at the APOL1 Locus.Ruchi, R., Genovese G., Lee J., Charoonratana VT, Bernhardy AJ, Alper SL, Kopp JB, Thadhani R., Friedman DJ, and Pollak MR PloS one, 2015/01/01, Volume 10, Issue 5, p.e0125410, (2015) Read More / View Supplemental Materials
Abstract
2014
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence.Genovese, G., Kähler AK, Handsaker RE, Lindberg J., Rose SA, Bakhoum SF, Chambert K., Mick E., Neale BM, Fromer M., Purcell SM, Svantesson O., Landén M., Höglund M., Lehmann S., Gabriel SB, Moran JL, Lander E. S., Sullivan PF, Sklar P., et al. The New England journal of medicine, 2014/11/26, (2014) Read More / View Supplemental Materials
Abstract
No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia.Ruderfer, DM, Lim ET, Genovese G., Moran JL, Hultman CM, Sullivan PF, McCarroll SA, Holmans P., Sklar P., and Purcell SM European journal of human genetics : EJHG, 2014/11/05, (2014) Read More / View Supplemental Materials
Abstract
Discovery of new glomerular disease-relevant genes by translational profiling of podocytes in vivo.Grgic, I., Hofmeister AF, Genovese G., Bernhardy AJ, Sun H., Maarouf OH, Bijol V., Pollak MR, and Humphreys BD Kidney international, 2014/06/18, (2014) Read More / View Supplemental Materials
Abstract
MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets.Strazisar, M., Cammaerts S., van der Ven K., Forero DA, Lenaerts AS, Nordin A., Almeida-Souza L., Genovese G., Timmerman V., Liekens A., De Rijk P., Adolfsson R., Callaerts P., and Del-Favero J. Molecular psychiatry, 2014/06/03, (2014) Read More / View Supplemental Materials
Abstract
A polygenic burden of rare disruptive mutations in schizophrenia.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., et al. Nature, 2014/02/13, Volume 506, Issue 7487, p.185-90, (2014) Read More / View Supplemental Materials
Abstract
Evidence that duplications of 22q11.2 protect against schizophrenia.Rees, E., Kirov G., Sanders A., Walters JT, Chambert KD, Shi J., Szatkiewicz J., O'Dushlaine C., Richards AL, Green EK, Jones I., Davies G., Legge SE, Moran JL, Pato C., Pato M., Genovese G., Levinson D., Duan J., Moy W., et al. Molecular psychiatry, 2014/01/01, Volume 19, Issue 1, p.37-40, (2014) Read More / View Supplemental Materials
Abstract
2013
The somatic genomic landscape of glioblastoma.Brennan, CW, Verhaak RG, McKenna A., Campos B., Noushmehr H., Salama SR, Zheng S., Chakravarty D., Sanborn JZ, Berman SH, Beroukhim R., Bernard B., Wu CJ, Genovese G., Shmulevich I., Barnholtz-Sloan J., Zou L., Vegesna R., Shukla SA, Ciriello G., et al. Cell, 2013/10/10, Volume 155, Issue 2, p.462-77, (2013) Read More / View Supplemental Materials
Abstract
Mapping the Human Reference Genome's Missing Sequence by Three-Way Admixture in Latino Genomes.Genovese, G., Handsaker RE, Li H., Kenny EE, and McCarroll SA American journal of human genetics, 2013/09/05, Volume 93, Issue 3, p.411-21, (2013) Read More / View Supplemental Materials
Abstract
Using population admixture to help complete maps of the human genome.Genovese, G., Handsaker RE, Li H., Altemose N., Lindgren AM, Chambert K., Pasaniuc B., Price AL, Reich D., Morton CC, Pollak MR, Wilson JG, and McCarroll SA Nature genetics, 2013/02/24, (2013) Read More / View Supplemental Materials
Abstract
APOL1 variants and kidney disease in people of recent African ancestry.Genovese, G., Friedman DJ, and Pollak MR Nature reviews. Nephrology, 2013/02/12, Volume 9, Issue 4, p.240-4, (2013) Read More / View Supplemental Materials
Abstract
2012
Informed conditioning on clinical covariates increases power in case-control association studies.Zaitlen, N., Lindström S., Pasaniuc B., Cornelis M., Genovese G., Pollack S., Barton A., Bickeböller H., Bowden DW, Eyre S., Freedman BI, Friedman DJ, Field JK, Groop L., Haugen A., Heinrich J., Henderson BE, Hicks PJ, Hocking LJ, Kolonel LN, et al. PLoS genetics, 2012/11/01, Volume 8, Issue 11, p.e1003032, (2012) Read More / View Supplemental Materials
Abstract
  • Showing 1-20 of 20 Results