Exploring human biology with N-of-1 clinical trials

por Schork, N. J., Beaulieu-Jones, B., Liang, W. S., Smalley, S., Goetz, L. H.
Publicado 2023

Two separate, large cohorts reveal potential modifiers of age-associated variation in visual reaction time performance

por Talboom, J. S., De Both, M. D., Naymik, M. A., Schmidt, A. M., Lewis, C. R., Jepsen, W. M., Håberg, A. K., Rundek, T., Levin, B. E., Hoscheidt, S., Bolla, Y., Brinton, R. D., Schork, N. J., Hay, M., Barnes, C. A., Glisky, E., Ryan, L., Huentelman, M. J.
Publicado 2021

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction

por Ayalew, M, Le-Niculescu, H, Levey, D F, Jain, N, Changala, B, Patel, S D, Winiger, E, Breier, A, Shekhar, A, Amdur, R, Koller, D, Nurnberger, J I, Corvin, A, Geyer, M, Tsuang, M T, Salomon, D, Schork, N J, Fanous, A H, O'Donovan, M C, Niculescu, A B
Publicado 2012

Precision medicine for suicidality: from universality to subtypes and personalization

por Niculescu, A B, Le-Niculescu, H, Levey, D F, Phalen, P L, Dainton, H L, Roseberry, K, Niculescu, E M, Niezer, J O, Williams, A, Graham, D L, Jones, T J, Venugopal, V, Ballew, A, Yard, M, Gelbart, T, Kurian, S M, Shekhar, A, Schork, N J, Sandusky, G E, Salomon, D R
Publicado 2017

Discovery and validation of blood biomarkers for suicidality

por Le-Niculescu, H, Levey, D F, Ayalew, M, Palmer, L, Gavrin, L M, Jain, N, Winiger, E, Bhosrekar, S, Shankar, G, Radel, M, Bellanger, E, Duckworth, H, Olesek, K, Vergo, J, Schweitzer, R, Yard, M, Ballew, A, Shekhar, A, Sandusky, G E, Schork, N J, Kurian, S M, Salomon, D R, Niculescu, A B
Publicado 2013

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease

por Vélez, J I, Chandrasekharappa, S C, Henao, E, Martinez, A F, Harper, U, Jones, M, Solomon, B D, Lopez, L, Garcia, G, Aguirre-Acevedo, D C, Acosta-Baena, N, Correa, J C, Lopera-Gómez, C M, Jaramillo-Elorza, M C, Rivera, D, Kosik, K S, Schork, N J, Swanson, J M, Lopera, F, Arcos-Burgos, M
Publicado 2013

Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach

por Niculescu, A B, Levey, D F, Phalen, P L, Le-Niculescu, H, Dainton, H D, Jain, N, Belanger, E, James, A, George, S, Weber, H, Graham, D L, Schweitzer, R, Ladd, T B, Learman, R, Niculescu, E M, Vanipenta, N P, Khan, F N, Mullen, J, Shankar, G, Cook, S, Humbert, C, Ballew, A, Yard, M, Gelbart, T, Shekhar, A, Schork, N J, Kurian, S M, Sandusky, G E, Salomon, D R
Publicado 2015

Genome-wide association study of shared components of reading disability and language impairment

por Eicher, J D, Powers, N R, Miller, L L, Akshoomoff, N, Amaral, D G, Bloss, C S, Libiger, O, Schork, N J, Darst, B F, Casey, B J, Chang, L, Ernst, T, Frazier, J, Kaufmann, W E, Keating, B, Kenet, T, Kennedy, D, Mostofsky, S, Murray, S S, Sowell, E R, Bartsch, H, Kuperman, J M, Brown, T T, Hagler, D J, Dale, A M, Jernigan, T L, St Pourcain, B, Davey Smith, G, Ring, S M, Gruen, J R
Publicado 2013

Evidence for the role of EPHX2 gene variants in anorexia nervosa

por Scott-Van Zeeland, A A, Bloss, C S, Tewhey, R, Bansal, V, Torkamani, A, Libiger, O, Duvvuri, V, Wineinger, N, Galvez, L, Darst, B F, Smith, E N, Carson, A, Pham, P, Phillips, T, Villarasa, N, Tisch, R, Zhang, G, Levy, S, Murray, S, Chen, W, Srinivasan, S, Berenson, G, Brandt, H, Crawford, S, Crow, S, Fichter, M M, Halmi, K A, Johnson, C, Kaplan, A S, La Via, M, Mitchell, J E, Strober, M, Rotondo, A, Treasure, J, Woodside, D B, Bulik, C M, Keel, P, Klump, K L, Lilenfeld, L, Plotnicov, K, Topol, E J, Shih, P B, Magistretti, P, Bergen, A W, Berrettini, W, Kaye, W, Schork, N J
Publicado 2014