Omer Weissbrod

Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease.

Kim SS, Dey KK, Weissbrod O, Márquez-Luna C, Gazal S, Price AL.

Nat Commun. 2020 12 07. 11(1):6258. PMID: 33288751

Functionally informed fine-mapping and polygenic localization of complex trait heritability.

Weissbrod O, Hormozdiari F, Benner C, Cui R, Ulirsch J, Gazal S, Schoech AP, van de Geijn B, Reshef Y, Márquez-Luna C, O'Connor L, Pirinen M, Finucane HK, Price AL.

Nat Genet. 2020 12. 52(12):1355-1363. PMID: 33199916

A reference map of potential determinants for the human serum metabolome.

Bar N, Korem T, Weissbrod O, Zeevi D, Rothschild D, Leviatan S, Kosower N, Lotan-Pompan M, Weinberger A, Le Roy CI, Menni C, Visconti A, Falchi M, Spector TD, Adamski J, Franks PW, Pedersen O, Segal E.

Nature. 2020 12. 588(7836):135-140. PMID: 33177712

Functional disease architectures reveal unique biological role of transposable elements.

Hormozdiari F, van de Geijn B, Nasser J, Weissbrod O, Gazal S, Ju CJ, Connor LO, Hujoel MLA, Engreitz J, Hormozdiari F, Price AL.

Nat Commun. 2019 09 06. 10(1):4054. PMID: 31492842

Estimating variance components in population scale family trees.

Shor T, Kalka I, Geiger D, Erlich Y, Weissbrod O.

PLoS Genet. 2019 05. 15(5):e1008124. PMID: 31071088

Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests.

Schweiger R, Fisher E, Weissbrod O, Rahmani E, Müller-Nurasyid M, Kunze S, Gieger C, Waldenberger M, Rosset S, Halperin E.

Nat Commun. 2018 11 21. 9(1):4919. PMID: 30464216

Prediction of acute myeloid leukaemia risk in healthy individuals.

Abelson S, Collord G, Ng SWK, Weissbrod O, Mendelson Cohen N, Niemeyer E, Barda N, Zuzarte PC, Heisler L, Sundaravadanam Y, Luben R, Hayat S, Wang TT, Zhao Z, Cirlan I, Pugh TJ, Soave D, Ng K, Latimer C, Hardy C, Raine K, Jones D, Hoult D, Britten A, McPherson JD, Johansson M, Mbabaali F, Eagles J, Miller JK, Pasternack D, Timms L, Krzyzanowski P, Awadalla P, Costa R, Segal E, Bratman SV, Beer P, Behjati S, Martincorena I, Wang JCY, Bowles KM, Quirós JR, Karakatsani A, La Vecchia C, Trichopoulou A, Salamanca-Fernández E, Huerta JM, Barricarte A, Travis RC, Tumino R, Masala G, Boeing H, Panico S, Kaaks R, Krämer A, Sieri S, Riboli E, Vineis P, Foll M, McKay J, Polidoro S, Sala N, Khaw KT, Vermeulen R, Campbell PJ, Papaemmanuil E, Minden MD, Tanay A, Balicer RD, Wareham NJ, Gerstung M, Dick JE, Brennan P, Vassiliou GS, Shlush LI.

Nature. 2018 07. 559(7714):400-404. PMID: 29988082

Estimating SNP-Based Heritability and Genetic Correlation in Case-Control Studies Directly and with Summary Statistics.

Weissbrod O, Flint J, Rosset S.

Am J Hum Genet. 2018 07 05. 103(1):89-99. PMID: 29979983

Host genetics and microbiome associations through the lens of genome wide association studies.

Weissbrod O, Rothschild D, Barkan E, Segal E.

Curr Opin Microbiol. 2018 08. 44:9-19. PMID: 29909175

Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype.

Shalata A, Mahroom M, Milewicz DM, Limin G, Kassum F, Badarna K, Tarabeih N, Assy N, Fell R, Cohen H, Nashashibi M, Livoff A, Azab M, Habib G, Geiger D, Weissbrod O, Nseir W.

Orphanet J Rare Dis. 2018 03 15. 13(1):41. PMID: 29544503