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A catalog of associations between rare coding variants and COVID-19 outcomes.

medRxiv : the preprint server for health sciences

Kosmicki JA, Horowitz JE, Banerjee N, Lanche R, Marcketta A, Maxwell E, Bai X, Sun D, Backman JD, Sharma D, Kang HM, O'Dushlaine C, Yadav A, Mansfield AJ, Li AH, Watanabe K, Gurski L, McCarthy SE, Locke AE, Khalid S, O'Keeffe S, Mbatchou J, Chazara O, Huang Y, Kvikstad E, O'Neill A, Nioi P, Parker MM, Petrovski S, Runz H, Szustakowski JD, Wang Q, Wong E, Cordova-Palomera A, Smith EN, Szalma S, Zheng X, Esmaeeli S, Davis JW, Lai YP, Chen X, Justice AE, Leader JB, Mirshahi T, Carey DJ, Verma A, Sirugo G, Ritchie MD, Rader DJ, Povysil G, Goldstein DB, Kiryluk K, Pairo-Castineira E, Rawlik K, Pasko D, Walker S, Meynert A, Kousathanas A, Moutsianas L, Tenesa A, Caulfield M, Scott R, Wilson JF, Baillie JK, Butler-Laporte G, Nakanishi T, Lathrop M, Richards JB, Jones M, Balasubramanian S, Salerno W, Shuldiner AR, Marchini J, Overton JD, Habegger L, Cantor MN, Reid JG, Baras A, Abecasis GR, Ferreira MA.
PMID: 33655273
medRxiv. 2021 Feb 27; doi: 10.1101/2020.10.28.20221804.

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) causes coronavirus disease-19 (COVID-19), a respiratory illness that can result in hospitalization or death. We investigated associations between rare genetic variants and seven COVID-19 outcomes in 543,213 individuals, including 8,248 with COVID-19. After...

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Kosmicki JA, Horowitz JE, Banerjee N, et al. A catalog of associations between rare coding variants and COVID-19 outcomes. medRxiv. 2021;doi: 10.1101/2020.10.28.20221804.
Kosmicki, J. A., Horowitz, J. E., Banerjee, N., Lanche, R., Marcketta, A., Maxwell, E., Bai, X., Sun, D., Backman, J. D., Sharma, D., Kang, H. M., O'Dushlaine, C., Yadav, A., Mansfield, A. J., Li, A. H., Watanabe, K., Gurski, L., McCarthy, S. E., Locke, A. E., Khalid, S., O'Keeffe, S., Mbatchou, J., Chazara, O., Huang, Y., Kvikstad, E., O'Neill, A., Nioi, P., Parker, M. M., Petrovski, S., Runz, H., Szustakowski, J. D., Wang, Q., Wong, E., Cordova-Palomera, A., Smith, E. N., Szalma, S., Zheng, X., Esmaeeli, S., Davis, J. W., Lai, Y. P., Chen, X., Justice, A. E., Leader, J. B., Mirshahi, T., Carey, D. J., Verma, A., Sirugo, G., Ritchie, M. D., Rader, D. J., Povysil, G., Goldstein, D. B., Kiryluk, K., Pairo-Castineira, E., Rawlik, K., Pasko, D., Walker, S., Meynert, A., Kousathanas, A., Moutsianas, L., Tenesa, A., Caulfield, M., Scott, R., Wilson, J. F., Baillie, J. K., Butler-Laporte, G., Nakanishi, T., Lathrop, M., Richards, J. B., Jones, M., Balasubramanian, S., Salerno, W., Shuldiner, A. R., Marchini, J., Overton, J. D., Habegger, L., Cantor, M. N., Reid, J. G., Baras, A., Abecasis, G. R., & Ferreira, M. A. (2021). A catalog of associations between rare coding variants and COVID-19 outcomes. medRxiv : the preprint server for health sciences, . https://doi.org/10.1101/2020.10.28.20221804
Kosmicki, J A, et al. "A catalog of associations between rare coding variants and COVID-19 outcomes." medRxiv : the preprint server for health sciences vol. (2021). doi: https://doi.org/10.1101/2020.10.28.20221804
Kosmicki JA, Horowitz JE, Banerjee N, Lanche R, Marcketta A, Maxwell E, Bai X, Sun D, Backman JD, Sharma D, Kang HM, O'Dushlaine C, Yadav A, Mansfield AJ, Li AH, Watanabe K, Gurski L, McCarthy SE, Locke AE, Khalid S, O'Keeffe S, Mbatchou J, Chazara O, Huang Y, Kvikstad E, O'Neill A, Nioi P, Parker MM, Petrovski S, Runz H, Szustakowski JD, Wang Q, Wong E, Cordova-Palomera A, Smith EN, Szalma S, Zheng X, Esmaeeli S, Davis JW, Lai YP, Chen X, Justice AE, Leader JB, Mirshahi T, Carey DJ, Verma A, Sirugo G, Ritchie MD, Rader DJ, Povysil G, Goldstein DB, Kiryluk K, Pairo-Castineira E, Rawlik K, Pasko D, Walker S, Meynert A, Kousathanas A, Moutsianas L, Tenesa A, Caulfield M, Scott R, Wilson JF, Baillie JK, Butler-Laporte G, Nakanishi T, Lathrop M, Richards JB, Jones M, Balasubramanian S, Salerno W, Shuldiner AR, Marchini J, Overton JD, Habegger L, Cantor MN, Reid JG, Baras A, Abecasis GR, Ferreira MA. A catalog of associations between rare coding variants and COVID-19 outcomes. medRxiv. 2021 Feb 27; doi: 10.1101/2020.10.28.20221804. PMID: 33655273; PMCID: PMC7924298.
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Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.

Molecular psychiatry

Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, Bromet EJ, Byerley W, Carvalho CB, Chapman SB, DeLisi LE, Dumont AL, O'Dushlaine C, Evgrafov OV, Fochtmann LJ, Gage D, Kennedy JL, Kinkead B, Macedo A, Moran JL, Morley CP, Dewan MJ, Nemesh J, Perkins DO, Purcell SM, Rakofsky JJ, Scolnick EM, Sklar BM, Sklar P, Smoller JW, Sullivan PF, Macciardi F, Marder SR, Gur RC, Gur RE, Braff DL, Nicolini H, Escamilla MA, Vawter MP, Sobell JL, Malaspina D, Lehrer DS, Buckley PF, Rapaport MH, Knowles JA, Fanous AH, Pato MT, McCarroll SA, Pato CN.
PMID: 31591465
Mol Psychiatry. 2020 Oct;25(10):2455-2467. doi: 10.1038/s41380-019-0517-y. Epub 2019 Oct 07.

Schizophrenia is a common, chronic and debilitating neuropsychiatric syndrome affecting tens of millions of individuals worldwide. While rare genetic variants play a role in the etiology of schizophrenia, most of the currently explained liability is within common variation, suggesting...

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Bigdeli TB, Genovese G, Georgakopoulos P, et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Mol Psychiatry. 2019;25(10):2455-2467doi: 10.1038/s41380-019-0517-y.
Bigdeli, T. B., Genovese, G., Georgakopoulos, P., Meyers, J. L., Peterson, R. E., Iyegbe, C. O., Medeiros, H., Valderrama, J., Achtyes, E. D., Kotov, R., Stahl, E. A., Abbott, C., Azevedo, M. H., Belliveau, R. A., Bevilacqua, E., Bromet, E. J., Byerley, W., Carvalho, C. B., Chapman, S. B., DeLisi, L. E., Dumont, A. L., O'Dushlaine, C., Evgrafov, O. V., Fochtmann, L. J., Gage, D., Kennedy, J. L., Kinkead, B., Macedo, A., Moran, J. L., Morley, C. P., Dewan, M. J., Nemesh, J., Perkins, D. O., Purcell, S. M., Rakofsky, J. J., Scolnick, E. M., Sklar, B. M., Sklar, P., Smoller, J. W., Sullivan, P. F., Macciardi, F., Marder, S. R., Gur, R. C., Gur, R. E., Braff, D. L., Nicolini, H., Escamilla, M. A., Vawter, M. P., Sobell, J. L., Malaspina, D., Lehrer, D. S., Buckley, P. F., Rapaport, M. H., Knowles, J. A., Fanous, A. H., Pato, M. T., McCarroll, S. A., & Pato, C. N. (2020). Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Molecular psychiatry, 25(10), 2455-2467. https://doi.org/10.1038/s41380-019-0517-y
Bigdeli, Tim B, et al. "Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry." Molecular psychiatry vol. 25,10 (2020): 2455-2467. doi: https://doi.org/10.1038/s41380-019-0517-y
Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, Bromet EJ, Byerley W, Carvalho CB, Chapman SB, DeLisi LE, Dumont AL, O'Dushlaine C, Evgrafov OV, Fochtmann LJ, Gage D, Kennedy JL, Kinkead B, Macedo A, Moran JL, Morley CP, Dewan MJ, Nemesh J, Perkins DO, Purcell SM, Rakofsky JJ, Scolnick EM, Sklar BM, Sklar P, Smoller JW, Sullivan PF, Macciardi F, Marder SR, Gur RC, Gur RE, Braff DL, Nicolini H, Escamilla MA, Vawter MP, Sobell JL, Malaspina D, Lehrer DS, Buckley PF, Rapaport MH, Knowles JA, Fanous AH, Pato MT, McCarroll SA, Pato CN. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Mol Psychiatry. 2020 Oct;25(10):2455-2467. doi: 10.1038/s41380-019-0517-y. Epub 2019 Oct 07. PMID: 31591465; PMCID: PMC7515843.
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Genome-wide analysis in 756,646 individuals provides first genetic evidence that .

medRxiv : the preprint server for health sciences

Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MA.
PMID: 33619501
medRxiv. 2021 Jun 10; doi: 10.1101/2020.12.14.20248176.

SARS-CoV-2 enters host cells by binding angiotensin-converting enzyme 2 (ACE2). Through a genome-wide association study, we show that a rare variant (MAF = 0.3%, odds ratio 0.60,

Cite
Horowitz JE, Kosmicki JA, Damask A, et al. Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv. 2021;doi: 10.1101/2020.12.14.20248176.
Horowitz, J. E., Kosmicki, J. A., Damask, A., Sharma, D., Roberts, G. H. L., Justice, A. E., Banerjee, N., Coignet, M. V., Yadav, A., Leader, J. B., Marcketta, A., Park, D. S., Lanche, R., Maxwell, E., Knight, S. C., Bai, X., Guturu, H., Sun, D., Baltzell, A., Kury, F. S. P., Backman, J. D., Girshick, A. R., O'Dushlaine, C., McCurdy, S. R., Partha, R., Mansfield, A. J., Turissini, D. A., Li, A. H., Zhang, M., Mbatchou, J., Watanabe, K., Gurski, L., McCarthy, S. E., Kang, H. M., Dobbyn, L., Stahl, E., Verma, A., Sirugo, G., Ritchie, M. D., Jones, M., Balasubramanian, S., Siminovitch, K., Salerno, W. J., Shuldiner, A. R., Rader, D. J., Mirshahi, T., Locke, A. E., Marchini, J., Overton, J. D., Carey, D. J., Habegger, L., Cantor, M. N., Rand, K. A., Hong, E. L., Reid, J. G., Ball, C. A., Baras, A., Abecasis, G. R., & Ferreira, M. A. (2021). Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv : the preprint server for health sciences, . https://doi.org/10.1101/2020.12.14.20248176
Horowitz, J E, et al. "Genome-wide analysis in 756,646 individuals provides first genetic evidence that ." medRxiv : the preprint server for health sciences vol. (2021). doi: https://doi.org/10.1101/2020.12.14.20248176
Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MA. Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv. 2021 Jun 10; doi: 10.1101/2020.12.14.20248176. PMID: 33619501; PMCID: PMC7899471.
Copy Download .nbib Format: NLM
Genome-wide analysis in 756,646 individuals provides first genetic evidence that .

medRxiv : the preprint server for health sciences

Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MA.
PMID: 33619501
medRxiv. 2021 Jun 10; doi: 10.1101/2020.12.14.20248176.

SARS-CoV-2 enters host cells by binding angiotensin-converting enzyme 2 (ACE2). Through a genome-wide association study, we show that a rare variant (MAF = 0.3%, odds ratio 0.60,

Cite
Horowitz JE, Kosmicki JA, Damask A, et al. Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv. 2021;doi: 10.1101/2020.12.14.20248176.
Horowitz, J. E., Kosmicki, J. A., Damask, A., Sharma, D., Roberts, G. H. L., Justice, A. E., Banerjee, N., Coignet, M. V., Yadav, A., Leader, J. B., Marcketta, A., Park, D. S., Lanche, R., Maxwell, E., Knight, S. C., Bai, X., Guturu, H., Sun, D., Baltzell, A., Kury, F. S. P., Backman, J. D., Girshick, A. R., O'Dushlaine, C., McCurdy, S. R., Partha, R., Mansfield, A. J., Turissini, D. A., Li, A. H., Zhang, M., Mbatchou, J., Watanabe, K., Gurski, L., McCarthy, S. E., Kang, H. M., Dobbyn, L., Stahl, E., Verma, A., Sirugo, G., Ritchie, M. D., Jones, M., Balasubramanian, S., Siminovitch, K., Salerno, W. J., Shuldiner, A. R., Rader, D. J., Mirshahi, T., Locke, A. E., Marchini, J., Overton, J. D., Carey, D. J., Habegger, L., Cantor, M. N., Rand, K. A., Hong, E. L., Reid, J. G., Ball, C. A., Baras, A., Abecasis, G. R., & Ferreira, M. A. (2021). Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv : the preprint server for health sciences, . https://doi.org/10.1101/2020.12.14.20248176
Horowitz, J E, et al. "Genome-wide analysis in 756,646 individuals provides first genetic evidence that ." medRxiv : the preprint server for health sciences vol. (2021). doi: https://doi.org/10.1101/2020.12.14.20248176
Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, Bai X, Guturu H, Sun D, Baltzell A, Kury FSP, Backman JD, Girshick AR, O'Dushlaine C, McCurdy SR, Partha R, Mansfield AJ, Turissini DA, Li AH, Zhang M, Mbatchou J, Watanabe K, Gurski L, McCarthy SE, Kang HM, Dobbyn L, Stahl E, Verma A, Sirugo G, Ritchie MD, Jones M, Balasubramanian S, Siminovitch K, Salerno WJ, Shuldiner AR, Rader DJ, Mirshahi T, Locke AE, Marchini J, Overton JD, Carey DJ, Habegger L, Cantor MN, Rand KA, Hong EL, Reid JG, Ball CA, Baras A, Abecasis GR, Ferreira MA. Genome-wide analysis in 756,646 individuals provides first genetic evidence that . medRxiv. 2021 Jun 10; doi: 10.1101/2020.12.14.20248176. PMID: 33619501; PMCID: PMC7899471.
Copy Download .nbib Format: NLM
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