Benjamin Neale

Munn-Chernoff, M. A., Johnson, E. C., Chou, Y. L., Coleman, J. R. I., Thornton, L. M., Walters, R. K., Yilmaz, Z., Baker, J. H., Hübel, C., Gordon, S., Medland, S. E., Watson, H. J., Gaspar, H. A., Bryois, J., Hinney, A., Leppä, V. M., Mattheisen, M., Ripke, S., Yao, S. & Giusti-Rodríguez, P. & 30 others, Hanscombe, K. B., Adan, R. A. H., Alfredsson, L., Ando, T., Andreassen, O. A., Berrettini, W. H., Boehm, I., Boni, C., Boraska Perica, V., Buehren, K., Burghardt, R., Cassina, M., Cichon, S., Clementi, M., Cone, R. D., Courtet, P., Crow, S., Farmer, A., Helder, S. G., Kalsi, G., McGuffin, P., Roberts, M., Schmidt, U., Treasure, J., Walton, E., Lynskey, M. T., Madden, P. A. F., Riley, B. P., Neale, B. M. & Breen, G., Jan 2021, In: Addiction Biology. 26, 1, e12880.

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37 Citations (Scopus)

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2020

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

The International Headache Genetics Consortium & the 23andMe Research Team, 1 Dec 2020, In: Nature Communications. 11, 1, 3368.

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46 Citations (Scopus)

Cerebral small vessel disease genomics and its implications across the lifespan

International Network against Thrombosis (INVENT) Consortium & International Headache Genomics Consortium (IHGC), Dec 2020, In: Nature Communications. 11, 1, 6285.

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122 Citations (Scopus)

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Eating Disorders Working Group of the Psychiatric Genomics Consortium, International Headache Genetics Consortium, 23andMe Research Team & Schmidt, U., 1 May 2020, In: Nature Genetics. 52, 5, p. 482-493 12 p.

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202 Citations (Scopus)

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Genome-wide association study identifies 48 common genetic variants associated with handedness

Cuellar-Partida, G., Tung, J. Y., Eriksson, N., Albrecht, E., Aliev, F., Andreassen, O. A., Barroso, I., Beckmann, J. S., Boks, M. P., Boomsma, D. I., Boyd, H. A., Breteler, M. M. B., Campbell, H., Chasman, D. I., Cherkas, L. F., Davies, G., de Geus, E. J. C., Deary, I. J., Deloukas, P. & Dick, D. M. & 98 others, Duffy, D. L., Eriksson, J. G., Esko, T., Feenstra, B., Geller, F., Gieger, C., Giegling, I., Gordon, S. D., Han, J., Hansen, T. F., Hartmann, A. M., Hayward, C., Heikkilä, K., Hicks, A. A., Hirschhorn, J. N., Hottenga, J. J., Huffman, J. E., Hwang, L. D., Ikram, M. A., Kaprio, J., Kemp, J. P., Khaw, K. T., Klopp, N., Konte, B., Kutalik, Z., Lahti, J., Li, X., Loos, R. J. F., Luciano, M., Magnusson, S. H., Mangino, M., Marques-Vidal, P., Martin, N. G., McArdle, W. L., McCarthy, M. I., Medina-Gomez, C., Melbye, M., Melville, S. A., Metspalu, A., Milani, L., Mooser, V., Nelis, M., Nyholt, D. R., O’Connell, K. S., Ophoff, R. A., Palmer, C., Palotie, A., Palviainen, T., Pare, G., Paternoster, L., Peltonen, L., Penninx, B. W. J. H., Polasek, O., Pramstaller, P. P., Prokopenko, I., Raikkonen, K., Ripatti, S., Rivadeneira, F., Rudan, I., Rujescu, D., Smit, J. H., Smith, G. D., Smoller, J. W., Soranzo, N., Spector, T. D., Pourcain, B. S., Starr, J. M., Stefánsson, H., Steinberg, S., Teder-Laving, M., Thorleifsson, G., Stefánsson, K., Timpson, N. J., Uitterlinden, A. G., van Duijn, C. M., van Rooij, F. J. A., Vink, J. M., Vollenweider, P., Vuoksimaa, E., Waeber, G., Wareham, N. J., Warrington, N., Waterworth, D., Werge, T., Wichmann, H. E., Widen, E., Willemsen, G., Wright, A. F., Wright, M. J., Xu, M., Zhao, J. H., Kraft, P., Hinds, D. A., Lindgren, C. M., Mägi, R., Neale, B. M., Evans, D. M. & Medland, S. E., 1 Jan 2020, (Accepted/In press) In: Nature Human Behaviour.

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97 Citations (Scopus)

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Genome Aggregation Database Production Team & Genome Aggregation Database Consortium, 1 Dec 2020, In: Nature Communications. 11, 1, 2539.

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101 Citations (Scopus)

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The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

Bipolar Disorder Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 15 Jul 2020, In: Biological psychiatry. 88, 2, p. 169-184 16 p.

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137 Citations (Scopus)

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2019

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Bipolar Disorder Working Group of the Psychiatric Genomics Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 1 Jan 2019, In: Molecular Psychiatry.

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31 Citations (Scopus)

Comparative genetic architectures of schizophrenia in East Asian and European populations

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Indonesia Schizophrenia Consortium & Genetic REsearch on schizophreniA neTwork-China and the Netherlands (GREAT-CN), 1 Dec 2019, In: Nature Genetics. 51, 12, p. 1670-1678 9 p.

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446 Citations (Scopus)

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, Demontis, D., Walters, R. K., Martin, J., Mattheisen, M., Als, T. D., Agerbo, E., Baldursson, G., Belliveau, R., Bybjerg-grauholm, J., Bækvad-hansen, M., Cerrato, F., Chambert, K., Churchhouse, C., Dumont, A., Eriksson, N., Gandal, M., Goldstein, J. I., Grasby, K. L. & Grove, J. & 32 others, Gudmundsson, O. O., Hansen, C. S., Hauberg, M. E., Hollegaard, M. V., Howrigan, D. P., Huang, H., Maller, J. B., Martin, A. R., Martin, N. G., Moran, J., Pallesen, J., Palmer, D. S., Pedersen, C. B., Pedersen, M. G., Poterba, T., Poulsen, J. B., Ripke, S., Robinson, E. B., Satterstrom, F. K., Stefansson, H., Stevens, C., Turley, P., Walters, G. B., Won, H., Wright, M. J., Andreassen, O. A., Asherson, P., Burton, C. L., Kuntsi, J., Sonuga-barke, E. J. S., Neale, B. M. & Plomin, R., 1 Jan 2019, In: Nature Genetics. 51, 1, p. 63-75 13 p.

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1391 Citations (Scopus)

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

ALSGENS Consortium, FALS Consortium, Project MinE Consortium, CReATe Consortium, Farhan, S. M. K., Howrigan, D. P., Abbott, L. E., Klim, J. R., Topp, S. D., Byrnes, A. E., Churchhouse, C., Phatnani, H., Smith, B. N., Rampersaud, E., Wu, G., Wuu, J., Shatunov, A., Iacoangeli, A., Al Khleifat, A. & Mordes, D. A. & 19 others, Ghosh, S., Eggan, K., Rademakers, R., McCauley, J. L., Schüle, R., Züchner, S., Benatar, M., Taylor, J. P., Nalls, M., Gotkine, M., Shaw, P. J., Morrison, K. E., Al-Chalabi, A., Traynor, B., Shaw, C. E., Goldstein, D. B., Harms, M. B., Daly, M. J. & Neale, B. M., 1 Dec 2019, In: Nature Neuroscience. 22, 12, p. 1966-1974 9 p.

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101 Citations (Scopus)

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

iPSYCH-GEMS Schizophrenia Working Group, CommonMind Consortium & The Schizophrenia Working Group of the PsyUniversity of Copenhagenchiatric Genomics Consortium, 1 Apr 2019, In: Nature Genetics. 51, 4, p. 659-674 16 p.

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135 Citations (Scopus)

Genetic markers of ADHD-related variations in intracranial volume

Klein, M., Walters, R. K., Demontis, D., Stein, J. L., Hibar, D. P., Adams, H. H., Bralten, J., Mota, N. R., Schachar, R., Sonuga-Barke, E., Mattheisen, M., Neale, B. M., Thompson, P. M., Medland, S. E., Børglum, A. D., Faraone, S. V., Arias-Vasquez, A. & Franke, B., 1 Mar 2019, In: American Journal of Psychiatry. 176, 3, p. 228-238 11 p.

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64 Citations (Scopus)

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

Wellcome Trust Case Control Consortium, Cross-Disorder Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Psychosis Endophenotypes International Consortium, Lee, P. H., Anttila, V., Won, H., Feng, Y. C. A., Rosenthal, J., Zhu, Z., Tucker-Drob, E. M., Nivard, M. G., Grotzinger, A. D., Posthuma, D., Arranz, M. J., Asherson, P., Kuntsi, J., Hansen, T. F., Reichenberg, A. & Sandin, S. & 34 others, Clarke, T. K., Coleman, J. R. I., Gaspar, H. A., Gordon, S. D., Kandaswamy, R., Lewis, C. M., Mullins, N., Schofield, P. R., Vincent, J. B., Baker, J. H., Davis, O. S. P., Helder, S. G., Roberts, M., Schmidt, U., Treasure, J., Walton, E., Howard, D., Smith, D. J., Uher, R., Collier, D. A., Kelly, B. J., Knight, J., McDonald, C., Murphy, K. C., Murray, R. M., Riley, B., Sham, P. C., van Os, J., Hedderly, T., Heyman, I., Woods, M., Breen, G., Walters, J. T. R. & Neale, B. M., 12 Dec 2019, In: Cell. 179, 7, p. 1469-1482.e11

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815 Citations (Scopus)

Identification of common genetic risk variants for autism spectrum disorder

Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium & 23andMe Research Team, 25 Feb 2019, (E-pub ahead of print) In: Nature Genetics. 51, 3, p. 431-444 14 p.

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1432 Citations (Scopus)

2018

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

23 and Me Research Team, Psychiatric Genomics Consortium: ADHD Subgroup, iPSYCH–Broad ADHD Workgroup, Martin, J., Walters, R. K., Demontis, D., Mattheisen, M., Lee, S. H., Robinson, E., Brikell, I., Ghirardi, L., Larsson, H., Lichtenstein, P., Eriksson, N., Agee, M., Alipanahi, B., Auton, A., Bell, R. K., Bryc, K. & Elson, S. L. & 33 others, Fontanillas, P., Furlotte, N. A., Hinds, D. A., Hromatka, B. S., Huber, K. E., Kleinman, A., Litterman, N. K., McIntyre, M. H., Mountain, J. L., Northover, C. A. M., Pitts, S. J., Sathirapongsasuti, J. F., Sazonova, O. V., Shelton, J. F., Shringarpure, S., Tian, C., Tung, J. Y., Vacic, V., Wilson, C. H., Albayrak, Ö., Anney, R. J. L., Vasquez, A. A., Arranz, M. J., Asherson, P., Banaschewski, T. J., Bau, C., Biederman, J., Mortensen, P. B., Freitag, C., Kuntsi, J., Neale, B. M., Sonuga-Barke, E. J. S. & Yang, L., 15 Jun 2018, In: Biological psychiatry. 83, 12, p. 1044-1053 10 p.

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128 Citations (Scopus)

Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis

iPSYCH-Broad ASD Group, the IMAGEN consortium, 1 Dec 2018, In: Translational psychiatry. 8, 1, 204.

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18 Citations (Scopus)

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

the 23andMe Research Team, 1 Dec 2018, In: PLoS Genetics. 14, 12, e1007813.

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365 Citations (Scopus)

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

23andMe Research Team, 1 Dec 2018, In: Nature Neuroscience. 21, 12, p. 1656-1669 14 p.

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426 Citations (Scopus)

2017

Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis

PGC ADHD Working Group, PGC Bipolar Disorder Working Group, van Hulzen, K. J. E., Scholz, C. J., Franke, B., Ripke, S., Klein, M., McQuillin, A., Sonuga-Barke, E. J. S., Kelsoe, J. R., Landén, M., Andreassen, O. A., Lesch, K. P., Weber, H., Faraone, S. V., Arias-Vasquez, A., Reif, A., Anney, R. J. L., Vasquez, A. A. & Arranz, M. J. & 32 others, Asherson, P., Banaschewski, T. J., Bayés, M., Biederman, J., Buitelaar, J. K., Casas, M., Charach, A., Cormand, B., Crosbie, J., Dalsgaard, S., Daly, M. J., Doyle, A. E., Ebstein, R. P., Elia, J., Freitag, C., Kuntsi, J., Neale, B. M., Breen, G., Collier, D. A., Craig, D. W., Day, R., Elkin, A., Farmer, A., Kandaswamy, R., McGuffin, P., Purcell, S., Schofield, P. R., Smith, E. N., Vincent, J. B., Williamson, R., Xu, W. & Young, A. H., 1 Nov 2017, In: Biological psychiatry. 82, 9, p. 634-641 8 p.

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99 Citations (Scopus)

2016

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Paediatric Cohorts

Middeldorp, C. M., Hammerschlag, A. R., Ouwens, K. G., Groen-Blokhuis, M. M., St. Pourcain, B., Greven, C. U., Pappa, I., Tiesler, C. M. T., Ang, W., Nolte, I. M., Vilor-Tejedor, N., Bacelis, J., Ebejer, J. L., Zhao, H., Davies, G. E., Ehli, E. A., Evans, D. M., Fedko, I. O., Guxens, M. & Hottenga, J.-J. & 31 others, Hudziak, J. J., Jugessur, A., Kemp, J. P., Krapohl, E., Martin, N. G., Murcia, M., Myhre, R., Ormel, J., Ring, S. M., Standl, M., Stergiakouli, E., Stoltenberg, C., Thiering, E., Timpson, N. J., Trzaskowski, M., van der Most, P. J., Wang, C., Nyholt, D. R., Medland, S. E., Neale, B., Jacobsson, B., Sunyer, J., Hartman, C. A., Whitehouse, A. J. O., Pennell, C. E., Heinrich, J., Plomin, R., Smith, G. D., Tiemeier, H., Posthuma, D. & Boomsma, D. I., Oct 2016, In: Journal of the American Academy of Child and Adolescent Psychiatry. 55, 10, p. 896–905.e6

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95 Citations (Scopus)

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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

Bodea, C. A., Neale, B. M., Ripke, S., International IBD Genetics Consortium, Daly, M. J., Devlin, B. & Roeder, K., 14 Apr 2016, (E-pub ahead of print) In: American Journal of Human Genetics.

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13 Citations (Scopus)

Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept

Psychosis Endophenotypes International Consortium, 23 Feb 2016, In: Nature Neuroscience. 19, 3, p. 420-431 12 p.

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171 Citations (Scopus)

2015

Converging evidence does not support GIT1 as an ADHD risk gene

Psychiatric Genomics Consortium ADHD Working Group, Klein, M., van der Voet, M., Harich, B., van Hulzen, K. J. E., Onnink, A. M. H., Hoogman, M., Guadalupe, T., Zwiers, M., Groothuismink, J. M., Verberkt, A., Nijhof, B., Castells-Nobau, A., Faraone, S. V., Buitelaar, J. K., Schenck, A., Arias-Vasquez, A., Franke, B., Anney, R. J. L. & Vasquez, A. A. & 31 others, Asherson, P., Banaschewski, T., Bayés, M., Biederman, J., Casas, M., Charach, A., Cormand, B., Crosbie, J., Daly, M. J., Doyle, A. E., Ebstein, R. P., Elia, J., Freitag, C., Gill, M., Hakonarson, H., Hebebrand, J., Hinney, A., Holmans, P., Kent, L., Kuntsi, J., Lambregts-Rommelse, N., Langley, K., Lesch, K. P., Loo, S. K., McGough, J. J., Medland, S. E., Meyer, J., Mick, E., Miranda, A., Mulas, F. & Neale, B. M., 1 Sept 2015, In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 168, 6, p. 492-507 16 p.

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15 Citations (Scopus)

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD

Yu, D., Mathews, C. A., Scharf, J. M., Neale, B. M., Davis, L. K., Gamazon, E. R., Derks, E. M., Evans, P., Edlund, C. K., Crane, J., Fagerness, J. A., Osiecki, L., Gallagher, P., Gerber, G., Haddad, S., Illmann, C., McGrath, L. M., Mayerfeld, C., Arepalli, S. & Barlassina, C. & 135 others, Barr, C. L., Bellodi, L., Benarroch, F., Berrió, G. B., Bienvenu, O. J., Black, D. W., Bloch, M. H., Brentani, H., Bruun, R. D., Budman, C. L., Camarena, B., Campbell, D. D., Cappi, C., Silgado, J. C. C., Cavallini, M. C., Chavira, D. A., Chouinard, S., Cook, E. H., Cookson, M. R., Coric, V., Cullen, B., Cusi, D., Delorme, R., Denys, D., Dion, Y., Eapen, V., Egberts, K., Falkai, P., Fernandez, T., Fournier, E., Garrido, H., Geller, D., Gilbert, D. L., Girard, S. L., Grabe, H. J., Grados, M. A., Greenberg, B. D., Gross-Tsur, V., Grünblatt, E., Hardy, J., Heiman, G. A., Hemmings, S. M. J., Herrera, L. D., Hezel, D. M., Hoekstra, P. J., Jankovic, J., Kennedy, J. L., King, R. A., Konkashbaev, A. I., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J. F., Lennertz, L., Liu, C., Lochner, C., Lowe, T. L., Lupoli, S., Macciardi, F., Maier, W., Manunta, P., Marconi, M., McCracken, J. T., Mesa Restrepo, S. C., Moessner, R., Moorjani, P., Morgan, J., Muller, H., Murphy, D. L., Naarden, A. L., Nurmi, E., Ochoa, W. C., Ophoff, R. A., Pakstis, A. J., Pato, M. T., Pato, C. N., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S. L., Renner, T., Reus, V. I., Richter, M. A., Riddle, M. A., Robertson, M. M., Romero, R., Rosário, M. C., Rosenberg, D., Ruhrmann, S., Sabatti, C., Salvi, E., Sampaio, A. S., Samuels, J., Sandor, P., Service, S. K., Sheppard, B., Singer, H. S., Smit, J. H., Stein, D. J., Strengman, E., Tischfield, J. A., Turiel, M., Valencia Duarte, A. V., Vallada, H., Veenstra-VanderWeele, J., Walitza, S., Wang, Y., Weale, M., Weiss, R., Wendland, J. R., Westenberg, H. G. M., Shugart, Y. Y., Hounie, A. G., Miguel, E. C., Nicolini, H., Wagner, M., Ruiz-Linares, A., Cath, D. C., McMahon, W., Posthuma, D., Oostra, B. A., Nestadt, G., Rouleau, G. A., Purcell, S., Jenike, M. A., Heutink, P., Hanna, G. L., Conti, D. V., Arnold, P. D., Freimer, N. B., Stewart, S. E., Knowles, J. A., Cox, N. J. & Pauls, D. L., Jan 2015, In: The American Journal of Psychiatry. 172, 1, p. 82-93 12 p.

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122 Citations (Scopus)

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

Day, F. R., Ruth, K. S., Thompson, D. J., Lunetta, K. L., Pervjakova, N., Chasman, D. I., Stolk, L., Finucane, H. K., Sulem, P., Bulik-Sullivan, B., Esko, T., Johnson, A. D., Elks, C. E., Franceschini, N., He, C., Altmaier, E., Brody, J. A., Franke, L. L., Huffman, J. E. & Keller, M. F. & 227 others, McArdle, P. F., Nutile, T., Porcu, E., Robino, A., Rose, L. M., Schick, U. M., Smith, J. A., Teumer, A., Traglia, M., Vuckovic, D., Yao, J., Zhao, W., Albrecht, E., Amin, N., Corre, T., Hottenga, J.-J., Mangino, M., Smith, A. V., Tanaka, T., Abecasis, G. R., Andrulis, I. L., Anton-Culver, H., Antoniou, A. C., Arndt, V., Arnold, A. M., Barbieri, C., Beckmann, M. W., Beeghly-Fadiel, A., Benitez, J., Bernstein, L., Bielinski, S. J., Blomqvist, C., Boerwinkle, E., Bogdanova, N. V., Bojesen, S. E., Bolla, M. K., Borresen-Dale, A.-L., Boutin, T. S., Brauch, H., Brenner, H., Brüning, T., Burwinkel, B., Campbell, A., Campbell, H., Chanock, S. J., Chapman, J. R., Chen, Y.-D. I., Chenevix-Trench, G., Couch, F. J., Coviello, A. D., Cox, A., Czene, K., Darabi, H., De Vivo, I., Demerath, E. W., Dennis, J., Devilee, P., Dörk, T., Dos-Santos-Silva, I., Dunning, A. M., Eicher, J. D., Fasching, P. A., Faul, J. D., Figueroa, J., Flesch-Janys, D., Gandin, I., Garcia, M. E., García-Closas, M., Giles, G. G., Girotto, G. G., Goldberg, M. S., González-Neira, A., Goodarzi, M. O., Grove, M. L., Gudbjartsson, D. F., Guénel, P., Guo, X., Haiman, C. A., Hall, P., Hamann, U., Henderson, B. E., Hocking, L. J., Hofman, A., Homuth, G., Hooning, M. J., Hopper, J. L., Hu, F. B., Huang, J., Humphreys, K., Hunter, D. J., Jakubowska, A., Jones, S. E., Kabisch, M., Karasik, D., Knight, J. A., Kolcic, I., Kooperberg, C., Kosma, V.-M., Kriebel, J., Kristensen, V., Lambrechts, D., Langenberg, C., Li, J., Li, X., Lindström, S., Liu, Y., Luan, J., Lubinski, J., Mägi, R., Mannermaa, A., Manz, J., Margolin, S., Marten, J., Martin, N. G., Masciullo, C., Meindl, A., Michailidou, K., Mihailov, E., Milani, L., Milne, R. L., Müller-Nurasyid, M., Nalls, M., Neale, B. M., Nevanlinna, H., Neven, P., Newman, A. B., Nordestgaard, B. G., Olson, J. E., Padmanabhan, S., Peterlongo, P., Peters, U., Petersmann, A., Peto, J., Pharoah, P. D. P., Pirastu, N. N., Pirie, A., Pistis, G., Polasek, O., Porteous, D., Psaty, B. M., Pylkäs, K., Radice, P., Raffel, L. J., Rivadeneira, F., Rudan, I., Rudolph, A., Ruggiero, D., Sala, C. F., Sanna, S., Sawyer, E. J., Schlessinger, D., Schmidt, M. K., Schmidt, F., Schmutzler, R. K., Schoemaker, M. J., Scott, R. A., Seynaeve, C. M., Simard, J., Sorice, R., Southey, M. C., Stöckl, D., Strauch, K., Swerdlow, A., Taylor, K. D., Thorsteinsdottir, U., Toland, A. E., Tomlinson, I., Truong, T., Tryggvadottir, L., Turner, S. T., Vozzi, D., Wang, Q., Wellons, M., Willemsen, G., Wilson, J. F., Winqvist, R., Wolffenbuttel, B. B. H. R., Wright, A. F., Yannoukakos, D., Zemunik, T., Zheng, W., Zygmunt, M., Bergmann, S., Boomsma, D. I., Buring, J. E., Ferrucci, L., Montgomery, G. W., Gudnason, V., Spector, T. D., van Duijn, C. M., Alizadeh, B. Z., Ciullo, M., Crisponi, L., Easton, D. F., Gasparini, P. P., Gieger, C., Harris, T. B., Hayward, C., Kardia, S. L. R., Kraft, P., McKnight, B., Metspalu, A., Morrison, A. C., Reiner, A. P., Ridker, P. M., Rotter, J. I., Toniolo, D., Uitterlinden, A. G., Ulivi, S., Völzke, H., Wareham, N. J., Weir, D. R., Yerges-Armstrong, L. M., Consortium, P., Investigators, K., Investigators, A., Scotland, G., Consortium, E.-I., Study, L. C., Price, A. L., Stefansson, K., Visser, J. A., Ong, K. K., Chang-Claude, J., Murabito, J. M., Perry, J. R. B. & Murray, A., Nov 2015, In: Nature Genetics. 47, 11, p. 1294—1303

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2014

Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder

Hart, A. B., Gamazon, E. R., Engelhardt, B. E., Sklar, P., Kähler, A. K., Hultman, C. M., Sullivan, P. F., Neale, B. M., Faraone, S. V., de Wit, H., Cox, N. J., Palmer, A. A. & Psychiatric Genomics Consortium: ADHD Subgroup, 22 Apr 2014, In: Proceedings of the National Academy of Sciences of the United States of America. 111, 16, p. 5968-5973 6 p.

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14 Citations (Scopus)

2013

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E. & Asherson, P. & 31 others, Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Breen, G., Collier, D. A., Craig, D. W., Craig, I. W., Day, R., Farmer, A. E., Fombonne, E., Freitag, C. M., Kuntsi, J., Lewis, C. M., Lowe, J. K., McGuffin, P., Parr, J. R., Sonuga-Barke, E. J. S., Young, A. H. & Cross-Disorder Group of the Psychiatric Genomics Consortium, Sept 2013, In: Nature Genetics. 45, 9, p. 984-994 11 p., N/A.

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1800 Citations (Scopus)

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Ripke, S., O'dushlaine, C., Chambert, K., Moran, J. L., K??hler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F. & Borglum, A. D. & 15 others, Bulik-sullivan, B. K., Cormican, P., Craddock, N., De Leeuw, C., Durmishi, N., Gill, M., Lin, K., Neale, B. M., Powell, J., Riley, B. P., Walters, J. T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Consortium 2 & Purcell, S., Oct 2013, In: Nature Genetics. 45, 10, p. 1150-1159 10 p.

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1228 Citations (Scopus)

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Anttila, V., Winsvold, B. S., Gormley, P., Kurth, T., Bettella, F., McMahon, G., Kallela, M., Malik, R., de Vries, B., Terwindt, G., Medland, S. E., Todt, U., McArdle, W. L., Quaye, L., Koiranen, M., Ikram, M. A., Lehtimäki, T., Stam, A. H., Ligthart, L. & Wedenoja, J. & 31 others, Dunham, I., Neale, B. M., Palta, P., Hamalainen, E., Schürks, M., Rose, L. M., Buring, J. E., Ridker, P. M., Steinberg, S., Stefansson, H., Jakobsson, F., Lawlor, D. A., Evans, D. M., Ring, S. M., Färkkilä, M., Artto, V., Kaunisto, M. A., Freilinger, T., Schoenen, J., Frants, R. R., Pelzer, N., Weller, C. M., Zielman, R., Heath, A. C., Madden, P. A. F., Montgomery, G. W., Martin, N. G., Borck, G., Williams, F. M. K., Cherkas, L. & North American Brain Expression Consortium, Aug 2013, In: Nature Genetics. 45, 8, p. 912-917 6 p., N/A.

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331 Citations (Scopus)

High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression

Hamshere, M. L., Langley, K., Martin, J., Agha, S. S., Stergiakouli, E., Anney, R. J. L., Buitelaar, J., Faraone, S. V., Lesch, K.-P., Neale, B. M., Franke, B., Sonuga-Barke, E., Asherson, P., Merwood, A., Kuntsi, J., Medland, S. E., Ripke, S., Steinhausen, H.-C., Freitag, C. & Reif, A. & 22 others, Renner, T. J., Romanos, M., Romanos, J., Warnke, A., Meyer, J., Palmason, H., Vasquez, A. A., Lambregts-Rommelse, N., Roeyers, H., Biederman, J., Doyle, A. E., Hakonarson, H., Rothenberger, A., Banaschewski, T., Oades, R. D., McGough, J. J., Kent, L., Williams, N., Owen, M. J., Holmans, P., O'Donovan, M. C. & Thapar, A., 2013, (E-pub ahead of print) In: The American Journal of Psychiatry.

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115 Citations (Scopus)

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Smoller, J. W., Craddock, N., Kendler, K., Lee, P. H., Neale, B. M., Nurnberger, J. I., Ripke, S., Santangelo, S., Sullivan, P. F., Cross-Disorder Group of the Psychiatric Genomics Consortium & Kuntsi, J., 20 Apr 2013, In: The Lancet. 381, 9875, p. 1371-1379 9 p.

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2336 Citations (Scopus)

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants

Yang, L., Neale, B. M., Liu, L., Lee, S. H., Wray, N. R., Ji, N., Li, H., Qian, Q., Wang, D., Li, J., Faraone, S. V., Wang, Y., Doyle, A. E., Reif, A., Rothenberger, A., Franke, B., Sonuga-Barke, E. J. S., Steinhausen, H.-C., Buitelaar, J. K. & Kuntsi, J. & 31 others, Biederman, J., Lesch, K.-P., Kent, L., Asherson, P., Oades, R. D., Loo, S. K., Nelson, S. F., Faraone, S. V., Smalley, S. L., Banaschewski, T., Arias Vasquez, A., Todorov, A., Charach, A., Miranda, A., Warnke, A., Thapar, A., Neale, B. M., Cormand, B., Freitag, C., Mick, E., Mulas, F., Middleton, F., HakonarsonHakonarson, H., Palmason, H., Schäfer, H., Roeyers, H., McGough, J. J., Romanos, J., Crosbie, J., Meyer, J. & Psychiatric GWAS Consortium: ADHD Subgroup, Jul 2013, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 162, 5, p. 419-430 12 p., N/A.

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