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Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases (2014). Gusev A, Lee SH, Trynka G, Finucane H, Vilhjבlmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium, Kהhler AK, Hultman CM, Purcell SM, McCarroll SA, Daly M, Pasaniuc B, Sullivan PF, Neale BM, Wray NR, Raychaudhuri S, Price AL; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium. Am J Hum Genet. 95:535-52.

Biological insights from 108 schizophrenia-associated genetic loci (2014). Schizophrenia Working Group of the Psychiatric Genomics Consortium. Nature 511:421-7.

Excess of homozygosity in the major histocompatibility complex in schizophrenia (2014). Mukherjee S, Guha S, Ikeda M, Iwata N, Malhotra AK, Pe'er I, Darvasi A, Lencz T. Hum Mol Genet. 23:6088-95.

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes (2014). Vacic V, Ozelius LJ, Clark LN, Bar-Shira A, Gana-Weisz M, Gurevich T, Gusev A, Kedmi M, Kenny EE, Liu X, Mejia-Santana H, Mirelman A, Raymond D, Saunders-Pullman R, Desnick RJ, Atzmon G, Burns ER, Ostrer H, Hakonarson H, Bergman A, Barzilai N, Darvasi A, Peter I, Guha S, Lencz T, Giladi N, Marder K, Pe'er I, Bressman SB, Orr-Urtreger A. Hum Mol Genet. 23:4693-702.

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT) (2014). Lencz T, Knowles E, Davies G, Guha S, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, DeRosse P, Lundervold A, Steen VM, John M, Espeseth T, Rהikkצnen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Ikeda M, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Horan M, Donohoe G, Morris D, Corvin A, Gill M, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Hellard SL, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK. Mol Psychiatry. 19:168-74.

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder (2013). Lencz T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L, Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nצthen MM, Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisantי A, Gregersen PK, Pe'er I, Malhotra AK, Goldman D, Darvasi A. Nat Commun. 4:2739.

High rate of disease-related copy number variations in childhood onset schizophrenia (2014). Ahn K, Gotay N, Andersen TM, Anvari AA, Gochman P, Lee Y, Sanders S, Guha S, Darvasi A, Glessner JT, Hakonarson H, Lencz T, State MW, Shugart YY, Rapoport JL. Mol Psychiatry. 19:568-72.

Implication of a rare deletion at distal 16p11.2 in schizophrenia (2013). Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nצthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G; Molecular Genetics of Schizophrenia Consortium; Wellcome Trust Case Control Consortium 2. JAMA Psychiatry. 70:253-60.

The variance of identity-by-descent sharing in the Wright-Fisher model (2013). Carmi S, Palamara PF, Vacic V, Lencz T, Darvasi A, Pe'er I. Genetics. 193:911-28.

Length distributions of identity by descent reveal fine-scale demographic history (2012). Palamara PF, Lencz T, Darvasi A, Pe'er I. Hum Genet. 91:1150.

Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris (2012). Sarig O, Bercovici S, Zoller L, Goldberg I, Indelman M, Nahum S, Israeli S, Sagiv N, Martinez de Morentin H, Katz O, Baum S, Barzilai A, Trau H, Murrell DF, Bergman R, Hertl M, Rosenberg S, Nצthen MM, Skorecki K, Schmidt E, Zillikens D, Darvasi A, Geiger D, Rosset S, Ibrahim SM, Sprecher E. J Invest Dermatol. 32:1798-805.

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci (2012). Kenny EE, Pe'er I, Karban A, Ozelius L, Mitchell AA, Ng SM, Erazo M, Ostrer H, Abraham C, Abreu MT, Atzmon G, Barzilai N, Brant SR, Bressman S, Burns ER, Chowers Y, Clark LN, Darvasi A, Doheny D, Duerr RH, Eliakim R, Giladi N, Gregersen PK, Hakonarson H, Jones MR, Marder K, McGovern DP, Mulle J, Orr-Urtreger A, Proctor DD, Pulver A, Rotter JI, Silverberg MS, Ullman T, Warren ST, Waterman M, Zhang W, Bergman A, Mayer L, Katz S, Desnick RJ, Cho JH, Peter I. PLoS Genet. 8:e1002559.

Implications for health and disease in the genetic signature of the Ashkenazi Jewish population (2012). Guha S, Rosenfeld JA, Malhotra AK, Lee AT, Gregersen PK, Kane JM, Pe'er I, Darvasi A, Lencz T. Genome Biol. 13:R2.

The Architecture of Long-Range Haplotypes Shared within and across Populations (2012). Gusev A, Palamara PF, Aponte G, Zhuang Z, Darvasi A, Gregersen P, Pe'er I. Mol Biol Evol. 29:473-86.

Genetic architecture of prostate cancer in the Ashkenazi Jewish population (2011). Vijai J, Kirchhoff T, Gallagher D, Hamel N, Guha S, Darvasi A, Lencz T, Foulkes WD, Offit K, Klein RJ. Br J Cancer. 105:864-9.

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia (2011). Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, N?ethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS; GROUP investigators; International Schizophrenia Consortium. Mol Psychiatry. 16:1117-29.

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder (2009). Pisant? A, Bronstein M, Yakir B, Darvasi A. Psychiatr Genet. 19:212.

Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved? (2009). Baruch K, Silberberg G, Aviv A, Shamir E, Bening-Abu-Shach U, Baruch Y, Darvasi A, Navon R. Int J Neuropsychopharmacol. 12:885-94.

Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population (2008). Bronstein M, Pisant? A, Yakir B, Darvasi A. Human Genetics 124:101-104.

Identification of loci associated with schizophrenia by genome-wide association and follow-up (2008). O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, M?ller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV; Molecular Genetics of Schizophrenia Collaboration, Gejman PV, Sanders AR, Duan J, Levinson DF, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR, Cichon S, N?then MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ. Nature Genetics 40: 1053-1055.

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (2009). O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Giegling I, Hartmann AM, M?ller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Adolfsson R, Osby U, Terenius L, J?nsson EG, Cichon S, N?then MM, Gill M, Corvin AP, Rujescu D, Gejman PV, Kirov G, Craddock N, Williams NM, Owen MJ. Mol Psychiatry 14:30-6.

Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women (2008). Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A. PLoS Genet. 4(2):e28

Type 2 diabetes whole genome association study in four populations: the DiaGen consortium (2007). Salonen JT, Uimari P, Aalto JM, Pirskanen M, Kaikkonen J, Todorova B, Hypp?nen J, Korhonen VP, Asikainen J, Devine C, Tuomainen TP, Luedemann J, Nauck M, Kerner W, Stephens RH, New JP, Ollier WE, Gibson JM, Payton A, Horan MA, Pendleton N, Mahoney W, Meyre D, Delplanque J, Froguel P, Luzzatto O, Yakir B, Darvasi A. Am. J. Hum. Genet. 81:338-45.

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia (2006). Shifman S, Levit A, Chen ML, Chen CH, Bronstein M, Weizman A, Yakir B, Navon R, Darvasi A. Hum. Genet. 120:160-70.

Further tests of the association between schizophrenia and single nucleotide polymorphism markers at the catechol-O-methyltransferase locus in an Ashkenazi Jewish population using microsatellite markers (2005). Horowitz A, Shifman S, Rivlin N, Pisant? A, Darvasi A. Psych. Genet. 15:163-9.

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients (2005). Horowitz A, Shifman S, Rivlin N, Pisant? A, Darvasi A. Schiz. Res. 73:263-267.

COMT: a common susceptibility gene in bipolar disorder and schizophrenia (2004). Shifman S, Bronstein M, Sternfeld M, Pisant? A, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Yakir B, Zak NB, Darvasi A. Am. J. Med. Genet. B 128:61-4.

Linkage disequilibrium patterns of the human genome across populations (2003). Shifman S, Kuypers J, Kokoris M, Yakir B, Darvasi A. Hum. Mol. Genet. 12:771-776.

A highly significant association between a COMT haplotype and schizophrenia (2002). Shifman S, Bronstein M, Sternfeld M, Pisant?-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer L, Kotler L, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A. Am. J. Hum. Genet. 71:1296-1302.

The value of isolated populations (2001). Shifman S, Darvasi A. Nat. Genet. 28(4):309-10.