Recent advances in understanding of attention deficit hyperactivity disorder (ADHD): how genetics are shaping our conceptualization of this disorder

por Zayats, Tetyana, Neale, Benjamin M
Publicado 2020

Genome-wide association studies in ADHD

por Franke, Barbara, Neale, Benjamin M., Faraone, Stephen V.
Publicado 2009

Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries

por Chen, Siwei, Neale, Benjamin M., Berkovic, Samuel F.
Publicado 2023

Genetic research in autism spectrum disorders

por Robinson, Elise B., Neale, Benjamin M., Hyman, Steven E.
Publicado 2015

The IMAGE project: methodological issues for the molecular genetic analysis of ADHD

por Kuntsi, Jonna, Neale, Benjamin M, Chen, Wai, Faraone, Stephen V, Asherson, Philip
Publicado 2006

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

por Gupta, Rahul, Karczewski, Konrad J, Howrigan, Daniel, Neale, Benjamin M, Mootha, Vamsi K
Publicado 2021

Incorporating family history of disease improves polygenic risk scores in diverse populations

por Hujoel, Margaux L.A., Loh, Po-Ru, Neale, Benjamin M., Price, Alkes L.
Publicado 2022

Phenome-wide heritability analysis of the UK Biobank

por Ge, Tian, Chen, Chia-Yen, Neale, Benjamin M., Sabuncu, Mert R., Smoller, Jordan W.
Publicado 2017

Correction: Phenome-wide heritability analysis of the UK Biobank

por Ge, Tian, Chen, Chia-Yen, Neale, Benjamin M., Sabuncu, Mert R., Smoller, Jordan W.
Publicado 2018

Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder

por Bahl, Samira, Chiang, Colby, Beauchamp, Roberta L, Neale, Benjamin M, Daly, Mark J, Gusella, James F, Talkowski, Michael E, Ramesh, Vijaya
Publicado 2013

SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests

por Zhou, Wei, Bi, Wenjian, Zhao, Zhangchen, Dey, Kushal K., Jagadeesh, Karthik A., Karczewski, Konrad J., Daly, Mark J., Neale, Benjamin M., Lee, Seunggeun
Publicado 2022

Publisher Correction: SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests

por Zhou, Wei, Bi, Wenjian, Zhao, Zhangchen, Dey, Kushal K., Jagadeesh, Karthik A., Karczewski, Konrad J., Daly, Mark J., Neale, Benjamin M., Lee, Seunggeun
Publicado 2022

Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank

por Lassen, Frederik H., Venkatesh, Samvida S., Baya, Nikolas, Zhou, Wei, Bloemendal, Alex, Neale, Benjamin M., Kessler, Benedikt M., Whiffin, Nicola, Lindgren, Cecilia M., Palmer, Duncan S.
Publicado 2023

Discordant calls across genotype discovery approaches elucidate variants with systematic errors

por Atkinson, Elizabeth G., Artomov, Mykyta, Loboda, Alexander A., Rehm, Heidi L., MacArthur, Daniel G., Karczewski, Konrad J., Neale, Benjamin M., Daly, Mark J.
Publicado 2023

Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotides

por Zhang, Sidi, Samocha, Kaitlin E., Rivas, Manuel A., Karczewski, Konrad J., Daly, Emma, Schmandt, Ben, Neale, Benjamin M., MacArthur, Daniel G., Daly, Mark J.
Publicado 2018

CHARR efficiently estimates contamination from DNA sequencing data

por Lu, Wenhan, Gauthier, Laura D., Poterba, Timothy, Giacopuzzi, Edoardo, Goodrich, Julia K., Stevens, Christine R., King, Daniel, Daly, Mark J., Neale, Benjamin M., Karczewski, Konrad J.
Publicado 2023

Testing for an Unusual Distribution of Rare Variants

por Neale, Benjamin M., Rivas, Manuel A., Voight, Benjamin F., Altshuler, David, Devlin, Bernie, Orho-Melander, Marju, Kathiresan, Sekar, Purcell, Shaun M., Roeder, Kathryn, Daly, Mark J.
Publicado 2011

Estimating heritability and its enrichment in tissue-specific gene sets in admixed populations

por Luo, Yang, Li, Xinyi, Wang, Xin, Gazal, Steven, Mercader, Josep Maria, Neale, Benjamin M, Florez, Jose C, Auton, Adam, Price, Alkes L, Finucane, Hilary K, Raychaudhuri, Soumya
Publicado 2021

Ancestry: How researchers use it and what they mean by it

por Dauda, Bege, Molina, Santiago J., Allen, Danielle S., Fuentes, Agustin, Ghosh, Nayanika, Mauro, Madelyn, Neale, Benjamin M., Panofsky, Aaron, Sohail, Mashaal, Zhang, Sarah R., Lewis, Anna C. F.
Publicado 2023

A data-driven medication score predicts 10-year mortality among aging adults

por Häppölä, Paavo, Havulinna, Aki S., Tasa, Tõnis, Mars, Nina J., Perola, Markus, Kallela, Mikko, Milani, Lili, Koskinen, Seppo, Salomaa, Veikko, Neale, Benjamin M., Palotie, Aarno, Daly, Mark, Ripatti, Samuli
Publicado 2020