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2017

A Powerful Test for SNP Effects on Multivariate Binary Outcomes Using Kernel Machine Regression

Davenport, C. A., Maity, A., Sullivan, P. F. & Tzeng, J. Y. Mar 24 2017 (Accepted/In press) In : Statistics in Biosciences. p. 1-22 22 p.

Research output: Research - peer-reviewArticle

Kernel Machines
Binary Outcomes
Regression
Single Nucleotide Polymorphism
Polymorphism

Deep Sequencing of 71 Candidate Genes to Characterize Variation Associated with Alcohol Dependence

Clark, S. L. , McClay, J. L. , Adkins, D. E. , Kumar, G. , Aberg, K. A. , Nerella, S. , Xie, L. , Collins, A. L. , Crowley, J. J. , Quackenbush, C. R. , Hilliard, C. E. , Shabalin, A. A. , Vrieze, S. I. , Peterson, R. E. , Copeland, W. E. , Silberg, J. L. , McGue, M. , Maes, H. , Iacono, W. G. , Sullivan, P. F. & 2 others Costello, E. J. & van den Oord, E. J. Jan 1 2017 In : Alcoholism: Clinical and Experimental Research. 41, 4, p. 711-718 8 p.

Research output: Research - peer-reviewArticle

High-Throughput Nucleotide Sequencing
Alcoholism
Genes
Alcohols
Alcohol Dehydrogenase

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

Yilmaz, Z., Szatkiewicz, J. P., Crowley, J. J., Ancalade, N., Brandys, M. K., Van Elburg, A., De Kovel, C. G. F., Adan, R. A. H., Hinney, A., Hebebrand, J., Gratacos, M., Fernandez-Aranda, F., Escaramis, G., Gonzalez, J. R., Estivill, X., Zeggini, E., Sullivan, P. F. & Bulik, C. M. Jan 1 2017 In : Psychiatric Genetics. 27, 4, p. 152-158 7 p.

Research output: Research - peer-reviewArticle

Anorexia Nervosa
Psychiatry
Neurodevelopmental Disorders
Quality Control
Sample Size
2 Citations

Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

Liu, X., Finucane, H. K., Gusev, A., Bhatia, G., Gazal, S., O'Connor, L., Bulik-Sullivan, B., Wright, F. A., Sullivan, P. F., Neale, B. M. & Price, A. L. Apr 6 2017 In : American Journal of Human Genetics. 100, 4, p. 605-616 12 p.

Research output: Research - peer-reviewArticle

Gene Expression Regulation
Gene Expression
Histone Code
2 Citations

Obstetrical, pregnancy and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women

Meltzer-Brody, S., Maegbaek, M. L., Medland, S. E., Miller, W. C., Sullivan, P. & Munk-Olsen, T. Jun 1 2017 In : Psychological Medicine. 47, 8, p. 1427-1441 15 p.

Research output: Research - peer-reviewArticle

Postpartum Period
Psychiatry
Economics
Pregnancy
Incidence
1 Citations

Schizophrenia and the dynamic genome

Sullivan, P. F. Mar 2 2017 In : Genome Medicine. 9, 1, 22

Research output: Research - peer-reviewComment/debate

Schizophrenia
Genome
2016
1 Citations

Deep Sequencing of Three Loci Implicated in Large-Scale Genome-Wide Association Study Smoking Meta-Analyses

Clark, S. L., McClay, J. L., Adkins, D. E., Aberg, K. A., Kumar, G., Nerella, S., Xie, L., Collins, A. L., Crowley, J. J., Quakenbush, C. R., Hillard, C. E., Gao, G., Shabalin, A. A., Peterson, R. E., Copeland, W. E., Silberg, J. L., Maes, H., Sullivan, P. F., Elizabeth, J. C. & van den Oord, E. J. May 1 2016 In : Nicotine and Tobacco Research. 18, 5, p. 626-631 6 p.

Research output: Research - peer-reviewArticle

High-Throughput Nucleotide Sequencing
Genome-Wide Association Study
Gene Frequency
Meta-Analysis
Smoking
4 Citations

Heritability of perinatal depression and genetic overlap with nonperinatal depression

Viktorin, A., Meltzer-Brody, S., Kuja-Halkola, R., Sullivan, P. F., Landén, M., Lichtenstein, P. & Magnusson, P. K. E. Feb 1 2016 In : American Journal of Psychiatry. 173, 2, p. 158-165 8 p.

Research output: Research - peer-reviewArticle

Depression
Siblings
Postpartum Depression
Twin Studies
Counseling
57 Citations

Integrative approaches for large-scale transcriptome-wide association studies

Gusev, A. , Ko, A. , Shi, H. , Bhatia, G. , Chung, W. , Penninx, B. W. J. H. , Jansen, R. , De Geus, E. J. C. , Boomsma, D. I. , Wright, F. A. , Sullivan, P. F. , Nikkola, E. , Alvarez, M. , Civelek, M. , Lusis, A. J. , Lehtimäki, T. , Raitoharju, E. , Kähönen, M. , Seppälä, I. , Raitakari, O. T. & 5 others Kuusisto, J., Laakso, M., Price, A. L., Pajukanta, P. & Pasaniuc, B. Mar 1 2016 In : Nature Genetics. 48, 3, p. 245-252 8 p.

Research output: Research - peer-reviewArticle

Transcriptome
Gene Expression
Phenotype
Genes
Genome-Wide Association Study
8 Citations

Nationwide genomic study in Denmark reveals remarkable population homogeneity

Athanasiadis, G., Cheng, J. Y., Vilhjálmsson, B. J., Jørgensen, F. G., Als, T. D., Le Hellard, S., Espeseth, T., Sullivan, P. F., Hultman, C. M., Kjærgaard, P. C., Schierup, M. H. & Mailund, T. Oct 1 2016 In : Genetics. 204, 2, p. 711-722 12 p.

Research output: Research - peer-reviewArticle

Denmark
Population
Norway
Sweden
History

One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins

Magnusson, P. K. E., Lee, D., Chen, X., Szatkiewicz, J., Pramana, S., Teo, S., Sullivan, P. F., Feuk, L. & Pawitan, Y. Apr 1 2016 In : Twin Research and Human Genetics. 19, 2, p. 97-103 7 p.

Research output: Research - peer-reviewArticle

Monozygotic Twins
Genome
Exons
Dizygotic Twins
Twin Studies
16 Citations

Polygenic overlap between schizophrenia risk and antipsychotic response: A genomic medicine approach

Ruderfer, D. M., Charney, A. W., Readhead, B., Kidd, B. A., Kähler, A. K., Kenny, P. J., Keiser, M. J., Moran, J. L., Hultman, C. M., Scott, S. A., Sullivan, P. F., Purcell, S. M., Dudley, J. T. & Sklar, P. Apr 1 2016 In : The Lancet Psychiatry. 3, 4, p. 350-357 8 p.

Research output: Research - peer-reviewArticle

Antipsychotic Agents
Schizophrenia
Medicine
Genes
Therapeutics
9 Citations

Translating genome-wide association findings into new therapeutics for psychiatry

Breen, G., Li, Q., Roth, B. L., O'Donnell, P., Didriksen, M., Dolmetsch, R., O'Reilly, P. F., Gaspar, H. A., Manji, H., Huebel, C., Kelsoe, J. R., Malhotra, D., Bertolino, A., Posthuma, D., Sklar, P., Kapur, S., Sullivan, P. F., Collier, D. A. & Edenberg, H. J. Oct 26 2016 In : Nature Neuroscience. 19, 11, p. 1392-1396 5 p.

Research output: Research - peer-reviewReview article

Psychiatry
Genome
Therapeutics
Genome-Wide Association Study
Genomics
2 Citations

What next in schizophrenia genetics for the psychiatric genomics consortium?

Corvin, A. & Sullivan, P. F. May 1 2016 In : Schizophrenia Bulletin. 42, 3, p. 538-541 4 p.

Research output: Research - peer-reviewReview article

Genome-Wide Association Study
Genomics
Psychiatry
Schizophrenia
2015
10 Citations

A Multi-Megabase Copy Number Gain Causes Maternal Transmission Ratio Distortion on Mouse Chromosome 2

Didion, J. P. , Morgan, A. P. , Clayshulte, A. M. F. , Mcmullan, R. C. , Yadgary, L. , Petkov, P. M. , Bell, T. A. , Gatti, D. M. , Crowley, J. J. , Hua, K. , Aylor, D. L. , Bai, L. , Calaway, M. , Chesler, E. J. , French, J. E. , Geiger, T. R. , Gooch, T. J. , Garland, T. , Harrill, A. H. , Hunter, K. & 16 others McMillan, L., Holt, M., Miller, D. R., O'Brien, D. A., Paigen, K., Pan, W., Rowe, L. B., Shaw, G. D., Simecek, P., Sullivan, P. F., Svenson, K. L., Weinstock, G. M., Threadgill, D. W., Pomp, D., Churchill, G. A. & Pardo-Manuel de Villena, F. 2015 In : PLoS Genetics. 11, 2, p. 1-29 29 p., e1004850

Research output: Research - peer-reviewArticle

chromosomes
mice
Chromosomes, Human, Pair 2
Mothers
chromosome
51 Citations

Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

Crowley, J. J. , Zhabotynsky, V. , Sun, W. , Huang, S. , Pakatci, I. K. , Kim, Y. , Wang, J. R. , Morgan, A. P. , Calaway, J. D. , Aylor, D. L. , Yun, Z. , Bell, T. A. , Buus, R. J. , Calaway, M. E. , Didion, J. P. , Gooch, T. J. , Hansen, S. D. , Robinson, N. N. , Shaw, G. D. , Spence, J. S. & 21 others Quackenbush, C. R., Barrick, C. J., Nonneman, R. J., Kim, K., Xenakis, J., Xie, Y., Valdar, W., Lenarcic, A. B., Wang, W., Welsh, C. E., Fu, C. P., Zhang, Z., Holt, J., Guo, Z., Threadgill, D. W., Tarantino, L. M., Miller, D. R., Zou, F., McMillan, L., Sullivan, P. F. & De Villena, F. P. M. Jan 1 2015 In : Nature Genetics. 47, 4, p. 353-360 8 p.

Research output: Research - peer-reviewArticle

Allelic Imbalance
Alleles
Gene Expression
Genetic Transcription
Single Nucleotide Polymorphism
2 Citations

A New Method for Detecting Associations with Rare Copy-Number Variants

Tzeng, J. Y., Magnusson, P. K. E., Sullivan, P. F., Szatkiewicz, J. P. & The Swedish Schizophrenia Consortium Jan 1 2015 In : PLoS Genetics. 11, 10, e1005403

Research output: Research - peer-reviewArticle

effect
method
methodology
loci
testing
8 Citations

Biological pathways and networks implicated in psychiatric disorders

Sullivan, P. F. & Posthuma, D. Apr 1 2015 In : Current Opinion in Behavioral Sciences. 2, p. 58-68 11 p.

Research output: Research - peer-reviewReview article

Psychiatry
Genes
Multifactorial Inheritance
Bipolar Disorder
Schizophrenia
10 Citations

CNV concordance in 1,097 MZ twin pairs

Abdellaoui, A., Ehli, E. A., Hottenga, J. J., Weber, Z., Mbarek, H., Willemsen, G., Van Beijsterveldt, T., Brooks, A., Hudziak, J. J., Sullivan, P. F., De Geus, E. J., Davies, G. E. & Boomsma, D. I. Feb 11 2015 In : Twin Research and Human Genetics. 18, 1, p. 1-12 12 p.

Research output: Research - peer-reviewArticle

Monozygotic Twins
DNA
Cheek
Epithelium
Genes
6 Citations

Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use

Clark, S. L., Aberg, K. A., Nerella, S., Kumar, G., Mcclay, J. L., Chen, W., Xie, L. Y., Harada, A., Shabalin, A. A., Gao, G., Bergen, S. E., Hultman, C. M., Magnusson, P. K. E., Sullivan, P. F. & van den Oord, E. J. C. G. Aug 1 2015 In : Alcoholism: Clinical and Experimental Research. 39, 8, p. 1396-1405 10 p.

Research output: Research - peer-reviewArticle

Alcohols
Association reactions
Methylation
Single Nucleotide Polymorphism
Direction compound
6 Citations

Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes

Pers, T. H., Timshel, P., Ripke, S., Lent, S., Sullivan, P. F., O'Donovan, M. C., Franke, L., Hirschhorn, J. N. & Schizophrenia Working Group of the Psychiatric Genomics Consortium Aug 17 2015 In : Human Molecular Genetics. 25, 6, p. 1247-1254 8 p., ddw007

Research output: Research - peer-reviewArticle

Ion Channels
Schizophrenia
Genes
Odds Ratio
Post-Synaptic Density
5 Citations

Disruption of the MicroRNA 137 primary transcript results in early embryonic lethality in mice

Crowley, J. J., Collins, A. L., Lee, R. J., Nonneman, R. J., Farrell, M. S., Ancalade, N., Mugford, J. W., Agster, K. L., Nikolova, V. D., Moy, S. S. & Sullivan, P. F. Jan 1 2015 In : Biological Psychiatry. 77, 2, p. e5-e7

Research output: Research - peer-reviewLetter

Mammalian Embryo
Fetal Diseases
MicroRNAs
Inbred C57BL Mouse
Knockout Mice
8 Citations

Educational attainment influences levels of homozygosity through migration and assortative mating

Abdellaoui, A., Hottenga, J. J., Willemsen, G., Bartels, M., Van Beijsterveldt, T., Ehli, E. A., Davies, G. E., Brooks, A., Sullivan, P. F., Penninx, B. W. J. H., De Geus, E. J. & Boomsma, D. I. Mar 3 2015 In : PLoS ONE. 10, 3, e0118935

Research output: Research - peer-reviewArticle

assortative mating
homozygosity
education
ancestry
Education
1 Citations

Erratum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance (Nature Genetics (2015) 47 (353-360))

Crowley, J. J. , Zhabotynsky, V. , Sun, W. , Huang, S. , Pakatci, I. K. , Kim, Y. , Wang, J. R. , Morgan, A. P. , Calaway, J. D. , Aylor, D. L. , Yun, Z. , Bell, T. A. , Buus, R. J. , Calaway, M. E. , Didion, J. P. , Gooch, T. J. , Hansen, S. D. , Robinson, N. N. , Shaw, G. D. , Spence, J. S. & 21 others Quackenbush, C. R., Barrick, C. J., Nonneman, R. J., Kim, K., Xenakis, J., Xie, Y., Valdar, W., Lenarcic, A. B., Wang, W., Welsh, C. E., Fu, C. P., Zhang, Z., Holt, J., Guo, Z., Threadgill, D. W., Tarantino, L. M., Miller, D. R., Zou, F., McMillan, L., Sullivan, P. F. & De Villena, F. P. M. Jan 1 2015 In : Nature Genetics. 47, 6, 1 p.

Research output: Research - peer-reviewComment/debate

Allelic Imbalance
Alleles
Gene Expression
57 Citations

Evaluating historical candidate genes for schizophrenia

Farrell, M. S., Werge, T., Sklar, P., Owen, M. J., Ophoff, R. A., O'donovan, M. C., Corvin, A., Cichon, S. & Sullivan, P. F. Jan 1 2015 In : Molecular Psychiatry. 20, 5, p. 555-562 8 p.

Research output: Research - peer-reviewArticle

Schizophrenia
Genes
Genetic Association Studies
Meta-Analysis
Research Personnel
2 Citations

Fast eQTL Analysis for Twin Studies

Yin, Z., Xia, K., Chung, W., Sullivan, P. F. & Zou, F. Jul 1 2015 In : Genetic Epidemiology. 39, 5, p. 357-365 9 p.

Research output: Research - peer-reviewArticle

Twin Studies
Quantitative Trait Loci
Netherlands
Single Nucleotide Polymorphism
Psychiatry
1 Citations

Functional characterization of the PCLO p.Ser4814Ala variant associated with major depressive disorder reveals cellular but not behavioral differences

Giniatullina, A. , Maroteaux, G. , Geerts, C. J. , Koopmans, B. , Loos, M. , Klaassen, R. , Chen, N. , van der Schors, R. C. , van Nierop, P. , Li, K. W. , de Jong, J. , Altrock, W. D. , Cornelisse, L. N. , Toonen, R. F. , van der Sluis, S. , Sullivan, P. F. , Stiedl, O. , Posthuma, D. , Smit, A. B. , Groffen, A. J. & 1 others Verhage, M. Aug 6 2015 In : Neuroscience. 300, p. 518-538 21 p.

Research output: Research - peer-reviewArticle

Major Depressive Disorder
Phenotype
Calcium
Population
Genetic Heterogeneity
7 Citations

Genetics of disease: Associations with depression

Sullivan, P. F. Jul 30 2015 In : Nature. 523, 7562, p. 539-540 2 p.

Research output: Research - peer-reviewShort survey

nervous system disorder
neurology
womens health
genetic engineering
health risk
5 Citations

Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood

Adkins, D. E., Clark, S. L., Copeland, W. E., Kennedy, M., Conway, K., Angold, A., Maes, H., Liu, Y., Kumar, G., Erkanli, A., Patkar, A. A., Silberg, J., Brown, T. H., Fergusson, D. M., Horwood, L. J., Eaves, L., Van Den Oord, E. J. C. G., Sullivan, P. F. & Costello, E. J. Jan 1 2015 In : Twin Research and Human Genetics. 18, 4, p. 335-347 13 p.

Research output: Research - peer-reviewArticle

Meta-Analysis
Genome
Underage Drinking
Alcohol Drinking
Genotype
28 Citations

Heterogeneity of postpartum depression: A latent class analysis

Putnam, K. , Robertson-Blackmore, E. , Sharkey, K. , Payne, J. , Bergink, V. , Munk-Olsen, T. , Deligiannidis, K. , Altemus, M. , Newport, J. , Apter, G. , Devouche, E. , Vikorin, A. , Magnusson, P. , Lichtenstein, P. , Penninx, B. , Buist, A. , Bilszta, J. , O'Hara, M. , Stuart, S. , Brock, R. & 14 others Roza, S., Tiemeier, H., Guille, C., Neill Epperson, C., Kim, D., Schmidt, P., Martinez, P., Wisner, K. L., Stowe, Z., Jones, I., Rubinow, D., Sullivan, P., Meltzer-Brody, S. & Postpartum Depression: Action Towards Causes and Treatment (PACT) Consortium Jan 1 2015 In : The Lancet Psychiatry. 2, 1, p. 59-67 9 p.

Research output: Research - peer-reviewArticle

Postpartum Depression
Suicidal Ideation
Pregnancy Complications
Tuberculin
Postpartum Period
21 Citations

High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction

McClay, J. L., Shabalin, A. A., Dozmorov, M. G., Adkins, D. E., Kumar, G., Nerella, S., Clark, S. L., Bergen, S. E., Hultman, C. M., Magnusson, P. K. E., Sullivan, P. F., Aberg, K. A. & van den Oord, E. J. C. G. Dec 23 2015 In : Genome Biology. 16, 1, 291

Research output: Research - peer-reviewArticle

methylation
single nucleotide polymorphism
quantitative trait loci
genomics
blood
3 Citations

IsoDOT Detects Differential RNA-Isoform Expression/Usage With Respect to a Categorical or Continuous Covariate With High Sensitivity and Specificity

Sun, W., Liu, Y., Crowley, J. J., Chen, T. H., Zhou, H., Chu, H., Huang, S., Kuan, P. F., Li, Y., Miller, D., Shaw, G., Wu, Y., Zhabotynsky, V., McMillan, L., Zou, F., Sullivan, P. F. & De Villena, F. P. M. Jul 3 2015 In : Journal of the American Statistical Association. 110, 511, p. 975-986 12 p.

Research output: Research - peer-reviewArticle

Differential Expression
Categorical
Specificity
Covariates
Gene
218 Citations

Meta-analysis of the heritability of human traits based on fifty years of twin studies

Polderman, T. J. C., Benyamin, B., De Leeuw, C. A., Sullivan, P. F., Van Bochoven, A., Visscher, P. M. & Posthuma, D. Jan 1 2015 In : Nature Genetics. 47, 7, p. 702-709 8 p.

Research output: Research - peer-reviewArticle

Twin Studies
Meta-Analysis
Chromosome Mapping
Individuality
Publications
2 Citations

Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection

Lu, Z. H., Zhu, H., Knickmeyer, R. C., Sullivan, P. F., Williams, S. N. & Zou, F. Dec 1 2015 In : Genetic Epidemiology. 39, 8, p. 664-677 14 p.

Research output: Research - peer-reviewArticle

Genome-Wide Association Study
Single Nucleotide Polymorphism
Markov Chains
Phenotype
5 Citations

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

Ruderfer, D. M., Lim, E. T., Genovese, G., Moran, J. L., Hultman, C. M., Sullivan, P. F., McCarroll, S. A., Holmans, P., Sklar, P. & Purcell, S. M. Jan 1 2015 In : European Journal of Human Genetics. 23, 4, p. 555-557 3 p.

Research output: Research - peer-reviewArticle

Schizophrenia
Exome
Recessive Genes
Population Genetics
Autistic Disorder
46 Citations

Polygenic risk score, parental socioeconomic status, family history of psychiatric disorders, and the risk for schizophrenia: A Danish population-based study and meta-analysis

Agerbo, E., Sullivan, P. F., Vilhjálmsson, B. J., Pedersen, C. B., Mors, O., Børglum, A. D., Hougaard, D. M., Hollegaard, M. V., Meier, S., Mattheisen, M., Ripke, S., Wray, N. R. & Mortensen, P. B. Jul 1 2015 In : JAMA Psychiatry. 72, 7, p. 635-641 7 p.

Research output: Research - peer-reviewArticle

Social Class
Psychiatry
Meta-Analysis
Schizophrenia
Population
8 Citations

The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects

Peyrot, W. J. , Lee, S. H. , Milaneschi, Y. , Abdellaoui, A. , Byrne, E. M. , Esko, T. , De Geus, E. J. C. , Hemani, G. , Hottenga, J. J. , Kloiber, S. , Levinson, D. F. , Lucae, S. , Martin, N. G. , Medland, S. E. , Metspalu, A. , Milani, L. , Noethen, M. M. , Potash, J. B. , Rietschel, M. , Rietveld, C. A. & 301 others Ripke, S., Shi, J., Willemsen, G., Zhu, Z., Boomsma, D. I., Wray, N. R., Penninx, B. W. J. H., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., Blackwood, D. H., Cichon, S., Heath, A. C., Holsboer, F., Madden, P. A., McGuffin, P., Muglia, P., Pergadia, M. L., Lin, D., Müller-Myhsok, B., Steinberg, S., Grabe, H. J., Lichtenstein, P., Magnusson, P., Perlis, R. H., Preisig, M., Smoller, J. W., Stefansson, K., Uher, R., Kutalik, Z., Tansey, K. E., Teumer, A., Viktorin, A., Barnes, M. R., Bettecken, T., Binder, E. B., Breuer, R., Castro, V. M., Churchill, S. E., Coryell, W. H., Craddock, N., Craig, I. W., Czamara, D., Degenhardt, F., Farmer, A. E., Fava, M., Frank, J., Gainer, V. S., Gallagher, P. J., Gordon, S. D., Goryachev, S., Gross, M., Guipponi, M., Henders, A. K., Herms, S., Hickie, I. B., Hoefels, S., Hoogendijk, W., Iosifescu, D. V., Ising, M., Jones, I., Jones, L., Jung-Ying, T., Knowles, J. A., Kohane, I. S., Kohli, M. A., Korszun, A., Landen, M., Lawson, W. B., Lewis, G., Macintyre, D., Maier, W., Mattheisen, M., McGrath, P. J., McIntosh, A., McLean, A., Middeldorp, C. M., Middleton, L., Montgomery, G. M., Murphy, S. N., Nauck, M., Nolen, W. A., Nyholt, D. R., O'Donovan, M., Oskarsson, H., Pedersen, N., Scheftner, W. A., Schulz, A., Schulze, T. G., Shyn, S. I., Sigurdsson, E., Slager, S. L., Smit, J. H., Stefansson, H., Steffens, M., Thorgeirsson, T., Tozzi, F., Treutlein, J., Uhr, M., Van Den Oord, E. J., Van Grootheest, G., Völzke, H., Weilburg, J. B., Willemsen, G., Zitman, F. G., Neale, B., Daly, M., Sullivan, P. F., Agrawal, A., Albrecht, E., Z Alizadeh, B., Allik, J., Amin, N., Attia, J. R., Bandinelli, S., Barnard, J., Bastardot, F., E Baumeister, S., Beauchamp, J., Benjamin, D. J., Benke, K. S., Bennett, D. A., Berger, K., Bielak, L. F., Bierut, L. J., Boatman, J. A., Boyle, P. A., Bültmann, U., Campbell, H., Cesarini, D., Chabris, C. F., Cherkas, L., Chung, M. K., Conley, D., Cucca, F., Davey-Smith, G., Davies, G., De Andrade, M., De Jager, P. L., De Leeuw, C., De Neve, J. E., Deary, I. J., Dedoussis, G. V., Deloukas, P., Derringer, J., Dimitriou, M., Eiriksdottir, G., Eklund, N., Elderson, M. F., Eriksson, J. G., Evans, D. S., Evans, D. M., Faul, J. D., Fehrmann, R., Ferrucci, L., Fischer, K., Franke, L., Garcia, M. E., Gieger, C., Gjessing, H. K., Groenen, P. J. F., Grönberg, H., Gudnason, V., Hägg, S., Hall, P., Harris, J. R., Harris, J. M., Harris, T. B., Hastie, N. D., Hayward, C., Heath, A. C., Hernandez, D. G., Hoffmann, W., Hofman, A., Hofman, A., Holle, R., Holliday, E. G., Holzapfel, C., Iacono, W. G., Ibrahim-Verbaas, C. A., Illig, T., Ingelsson, E., Jacobsson, B., Järvelin, M. R., Jhun, M. A., Johannesson, M., Joshi, P. K., Jugessur, A., Kaakinen, M., Kähönen, M., Kanoni, S., Kaprio, J., Kardia, S. L. R., Karjalainen, J., Kirkpatrick, R. M., Koellinger, P. D., Kolcic, I., Kowgier, M., Kristiansson, K., Krueger, R. F., Kutalik, Z., Lahti, J., Laibson, D., Latvala, A., Launer, L. J., Lawlor, D. A., Lethimäki, T., Li, J., Lichtenstein, P., Lichtner, P. K., Liewald, D. C., Lin, P., Lind, P. A., Liu, Y., Lohman, K., Loitfelder, M., Madden, P. A., Magnusson, P. K. E., Mäkinen, T. E., Vidal, P. M., Martin, N. W., Masala, M., McGue, M., McMahon, G., Meirelles, O., Meyer, M. N., Mielck, A., Milani, L., Miller, M. B., Montgomery, G. W., Mukherjee, S., Myhre, R., Nuotio, M. L., Nyholt, D. R., J Oldmeadow, C., Oostra, B. A., Palmer, L. J., Palotie, A., Perola, M., Petrovic, K. E., Peyser, P. A., Polašek, O., Posthuma, D., Preisig, M., Quaye, L., Räikkönen, K., Raitakari, O. T., Realo, A., Reinmaa, E., Rice, J. P., Ring, S. M., Ripatti, S., Rivadeneira, F., Rizzi, T. S., Rudan, I., Rustichini, A., Salomaa, V., Sarin, A. P., Schlessinger, D., Schmidt, H., Schmidt, R., Scott, R. J., Shakhbazov, K., Smith, A. V., Smith, J. A., Snieder, H., St Pourcain, B., Starr, J. M., Sul, J. H., Surakka, I., Svento, R., Tanaka, T., Terracciano, A., Teumer, A., Thurik, A. R., Tiemeier, H., Timpson, N. J., Uitterlinden, A. G., Van Der Loos, M. J. H. M., Van Duijn, C. M., Van Rooij, F. J. A., Van Wagoner, D. R., Vartiainen, E., Viikari, J., Visscher, P. M., Vitart, V., Vollenweider, P. K., Völzke, H., Vonk, J. M., Waeber, G., Weir, D. R., Wellmann, J., Westra, H. J., Wichmann, H. E., Widen, E., Wilson, J. F., Wright, A. F., Yang, J., Yu, L. & Zhao, W. Jan 1 2015 In : Molecular Psychiatry. 20, 6, p. 735-743 9 p.

Research output: Research - peer-reviewArticle

Major Depressive Disorder
Depression
Single Nucleotide Polymorphism
Genomics
Mental Disorders
12 Citations

The Mouse Universal Genotyping Array: From Substrains to Subspecies

Morgan, A. P. , Fu, C. P. , Kao, C. Y. , Welsh, C. E. , Didion, J. P. , Yadgary, L. , Hyacinth, L. , Ferris, M. T. , Bell, T. A. , Miller, D. R. , Giusti-Rodriguez, P. , Nonneman, R. J. , Cook, K. D. , Whitmire, J. K. , Gralinski, L. E. , Keller, M. , Attie, A. D. , Churchill, G. A. , Petkov, P. , Sullivan, P. F. & 3 others Brennan, J. R., McMillan, L. & Pardo-Manuel de Villena, F. Dec 18 2015 In : G3 (Bethesda, Md.). 6, 2, p. 263-279 17 p.

Research output: Research - peer-reviewArticle

Population Genetics
Quality Control
Single Nucleotide Polymorphism
Genome
Population
2014
99 Citations

A genome-wide association study of anorexia nervosa

Boraska, V. , Franklin, C. S. , Floyd, J. A. B. , Thornton, L. M. , Huckins, L. M. , Southam, L. , Rayner, N. W. , Tachmazidou, I. , Klump, K. L. , Treasure, J. , Lewis, C. M. , Schmidt, U. , Tozzi, F. , Kiezebrink, K. , Hebebrand, J. , Gorwood, P. , Adan, R. A. H. , Kas, M. J. H. , Favaro, A. , Santonastaso, P. & 196 others Fernández-Aranda, F., Gratacos, M., Rybakowski, F., Dmitrzak-Weglarz, M., Kaprio, J., Keski-Rahkonen, A., Raevuori, A., Van Furth, E. F., Slof-Op 't Landt, M. C. T., Hudson, J. I., Reichborn-Kjennerud, T., Knudsen, G. P. S., Monteleone, P., Kaplan, A. S., Karwautz, A., Hakonarson, H., Berrettini, W. H., Guo, Y., Li, D., Schork, N. J., Komaki, G., Ando, T., Inoko, H., Esko, T., Fischer, K., Männik, K., Metspalu, A., Baker, J. H., Cone, R. D., Dackor, J., DeSocio, J. E., Hilliard, C. E., O'Toole, J. K., Pantel, J., Szatkiewicz, J. P., Taico, C., Zerwas, S., Trace, S. E., Davis, O. S. P., Helder, S., Bühren, K., Burghardt, R., De Zwaan, M., Egberts, K., Ehrlich, S., Herpertz-Dahlmann, B., Herzog, W., Imgart, H., Scherag, A., Scherag, S., Zipfel, S., Boni, C., Ramoz, N., Versini, A., Brandys, M. K., Danner, U. N., De Kovel, C., Hendriks, J., Koeleman, B. P. C., Ophoff, R. A., Strengman, E., Van Elburg, A. A., Bruson, A., Clementi, M., Degortes, D., Forzan, M., Tenconi, E., Docampo, E., Escaramís, G., Jiménez-Murcia, S., Lissowska, J., Rajewski, A., Szeszenia-Dabrowska, N., Slopien, A., Hauser, J., Karhunen, L., Meulenbelt, I., Slagboom, P. E., Tortorella, A., Maj, M., Dedoussis, G., Dikeos, D., Gonidakis, F., Tziouvas, K., Tsitsika, A., Papezova, H., Slachtova, L., Martaskova, D., Kennedy, J. L., Levitan, R. D., Yilmaz, Z., Huemer, J., Koubek, D., Merl, E., Wagner, G., Lichtenstein, P., Breen, G., Cohen-Woods, S., Farmer, A., McGuffin, P., Cichon, S., Giegling, I., Herms, S., Rujescu, D., Schreiber, S., Wichmann, H. E., Dina, C., Sladek, R., Gambaro, G., Soranzo, N., Julia, A., Marsal, S., Rabionet, R., Gaborieau, V., Dick, D. M., Palotie, A., Ripatti, S., Widén, E., Andreassen, O. A., Espeseth, T., Lundervold, A., Reinvang, I., Steen, V. M., Le Hellard, S., Mattingsdal, M., Ntalla, I., Bencko, V., Foretova, L., Janout, V., Navratilova, M., Gallinger, S., Pinto, D., Scherer, S. W., Aschauer, H., Carlberg, L., Schosser, A., Alfredsson, L., Ding, B., Klareskog, L., Padyukov, L., Courtet, P., Guillaume, S., Jaussent, I., Finan, C., Kalsi, G., Roberts, M., Logan, D. W., Peltonen, L., Ritchie, G. R. S., Barrett, J. C., Anderson, C. A., Barrett, J. C., Floyd, J. A. B., Franklin, C. S., McGinnis, R., Soranzo, N., Zeggini, E., Sambrook, J., Stephens, J., Ouwehand, W. H., McArdle, W. L., Ring, S. M., Strachan, D. P., Alexander, G., Bulik, C. M., Collier, D. A., Conlon, P. J., Dominiczak, A., Duncanson, A., Hill, A., Langford, C., Lord, G., Maxwell, A. P., Morgan, L., Peltonen, L., Sandford, R. N., Sheerin, N., Vannberg, F. O., Blackburn, H., Chen, W. M., Edkins, S., Gillman, M., Gray, E., Hunt, S. E., Onengut-Gumuscu, S., Potter, S., Rich, S. S., Simpkin, D., Whittaker, P., Estivill, X., Hinney, A., Sullivan, P. F., Collier, D. A., Zeggini, E., Bulik, C. M. & The Wellcome Trust Case Control Consortium 3 Oct 1 2014 In : Molecular Psychiatry. 19, 10, p. 1085-1094 10 p.

Research output: Research - peer-reviewArticle

Genome-Wide Association Study
Anorexia Nervosa
Datasets
Computer Simulation
Single Nucleotide Polymorphism
28 Citations

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

Li, M. , Luo, X. J. , Rietschel, M. , Lewis, C. M. , Mattheisen, M. , Müller-Myhsok, B. , Jamain, S. , Leboyer, M. , Landén, M. , Thompson, P. M. , Cichon, S. , Nöthen, M. M. , Schulze, T. G. , Sullivan, P. F. , Bergen, S. E. , Donohoe, G. , Morris, D. W. , Hargreaves, A. , Gill, M. , Corvin, A. & 28 others Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C., Etain, B., Bis, J. C., Ikram, M. A., Fornage, M., Debette, S., Launer, L. J., Seshadri, S., Erk, S., Walter, H., Heinz, A., Bellivier, F., Stein, J. L., Medland, S. E., Arias Vasquez, A., Hibar, D. P., Franke, B., Martin, N. G., Wright, M. J. & Su, B. Apr 1 2014 In : Molecular Psychiatry. 19, 4, p. 452-461 10 p.

Research output: Research - peer-reviewArticle

Gene Expression Regulation
Bipolar Disorder
Single Nucleotide Polymorphism
Population
Alleles
60 Citations

A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects

Mcclay, J. L., Aberg, K. A., Clark, S. L., Nerella, S., Kumar, G., Xie, L. Y., Hudson, A. D., Harada, A., Hultman, C. M., Magnusson, P. K. E., Sullivan, P. F. & Van den oord, E. J. C. G. Mar 2014 In : Human Molecular Genetics. 23, 5, p. 1175-1185 11 p., ddt511

Research output: Research - peer-reviewArticle

High-Throughput Nucleotide Sequencing
DNA
Methylation
Genes
Histone Code
10 Citations

An inherited duplication at the gene p21 protein-activated Kinase 7 (PAK7) is a risk factor for psychosis

Morris, D. W. , Pearson, R. D. , Cormican, P. , Kenny, E. M. , O'Dushlaine, C. T. , Perreault, L. P. L. , Giannoulatou, E. , Tropea, D. , Maher, B. S. , Wormley, B. , Kelleher, E. , Fahey, C. , Molinos, I. , Bellini, S. , Pirinen, M. , Strange, A. , Freeman, C. , Thiselton, D. L. , Elves, R. L. , Regan, R. & 36 others Ennis, S., Dinan, T. G., McDonald, C., Murphy, K. C., O'Callaghan, E., Waddington, J. L., Walsh, D., O'Donovan, M., Grozeva, D., Craddock, N., Stone, J., Scolnick, E., Purcell, S., Sklar, P., Coe, B., Eichler, E. E., Ophoff, R., Buizer, J., Szatkiewicz, J., Hultman, C., Sullivan, P., Gurling, H., Mcquillin, A., St Clair, D., Rees, E., Kirov, G., Walters, J., Blackwood, D., Johnstone, M., Donohoe, G., OwNeill, F. A., Kendler, K. S., Gill, M., Riley, B. P., Spencer, C. C. A. & Corvin, A. Jan 1 2014 In : Human Molecular Genetics. 23, 12, p. 3316-3326 11 p.

Research output: Research - peer-reviewArticle

p21-Activated Kinases
Psychotic Disorders
Protein Kinases
Schizophrenia
Proteins
8 Citations
RNA Sequence Analysis
RNA
X Chromosome
Gene Expression
Chromosomes
483 Citations

A polygenic burden of rare disruptive mutations in schizophrenia

Purcell, S. M. , Moran, J. L. , Fromer, M. , Ruderfer, D. , Solovieff, N. , Roussos, P. , O'Dushlaine, C. , Chambert, K. , Bergen, S. E. , Kähler, A. , Duncan, L. , Stahl, E. , Genovese, G. , Fernández, E. , Collins, M. O. , Komiyama, N. H. , Choudhary, J. S. , Magnusson, P. K. E. , Banks, E. , Shakir, K. & 12 others Garimella, K., Fennell, T., Depristo, M., Grant, S. G. N., Haggarty, S. J., Gabriel, S., Scolnick, E. M., Lander, E. S., Hultman, C. M., Sullivan, P. F., McCarroll, S. A. & Sklar, P. Jan 28 2014 In : Nature. 506, 7487, p. 185-190 6 p.

Research output: Research - peer-reviewArticle

Schizophrenia
Mutation
Genes
Exome
Alleles
14 Citations

Applying polygenic risk scores to postpartum depression

Byrne, E. M. , Carrillo-Roa, T. , Penninx, B. W. J. H. , Sallis, H. M. , Viktorin, A. , Chapman, B. , Henders, A. K. , Pergadia, M. L. , Heath, A. C. , Madden, P. A. F. , Sullivan, P. F. , Boschloo, L. , van Grootheest, G. , McMahon, G. , Lawlor, D. A. , Landén, M. , Lichtenstein, P. , Magnusson, P. K. E. , Evans, D. M. , Montgomery, G. W. & 4 others Boomsma, D. I., Martin, N. G., Meltzer-Brody, S. & Wray, N. R. Nov 20 2014 In : Archives of Women's Mental Health. 17, 6, p. 519-528 10 p.

Research output: Research - peer-reviewArticle

Postpartum Depression
Major Depressive Disorder
Bipolar Disorder
Genomics
Single Nucleotide Polymorphism
10 Citations

A recessive genetic model and runs of homozygosity in major depressive disorder

Power, R. A., Keller, M. C., Ripke, S., Abdellaoui, A., Wray, N. R., Sullivan, P. F. & Breen, G. Mar 2014 In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 165, 2, p. 157-166 10 p.

Research output: Research - peer-reviewArticle

Genome-Wide Association Study
Genetic Models
Major Depressive Disorder
Genome
Schizophrenia
1655 Citations

Biological insights from 108 schizophrenia-associated genetic loci

Ripke, S. , Neale, B. M. , Corvin, A. , Walters, J. T. R. , Farh, K. H. , Holmans, P. A. , Lee, P. , Bulik-Sullivan, B. , Collier, D. A. , Huang, H. , Pers, T. H. , Agartz, I. , Agerbo, E. , Albus, M. , Alexander, M. , Amin, F. , Bacanu, S. A. , Begemann, M. , Belliveau, R. A. , Bene, J. & 280 others Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chen, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Cloninger, C. R., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Degenhardt, F., Del Favero, J., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Frank, J., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Genovese, G., Georgieva, L., Giegling, I., Giusti-Rodríguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., De Haan, L., Hammer, C., Hamshere, M. L., Hansen, M., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Herms, S., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julià, A., Kahn, R. S., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Keller, M. C., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kähler, A. K., Laurent, C., Keong, J. L. C., Lee, S. H., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K. Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lönnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Maier, W., Mallet, J., Marsal, S., Mattheisen, M., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Müller-Myhsok, B., Nelis, M., Nenadic, I., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C., O'Neill, F. A., Oh, S. Y., Olincy, A., Olsen, L., Van Os, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietiläinen, O., Pimm, J., Pocklington, A. J., Powell, J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Ruderfer, D. M., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schulze, T. G., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stahl, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Strohmaier, J., Stroup, T. S., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Witt, S. H., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Cichon, S., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gill, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jönsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarroll, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Nöthen, M. M., Ophoff, R. A., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Rietschel, M., Riley, B. P., Rujescu, D., Sham, P. C., Sklar, P., St Clair, D., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., Sullivan, P. F. & O'Donovan, M. C. Jan 1 2014 In : Nature. 511, 7510, p. 421-427 7 p.

Research output: Research - peer-reviewArticle

Genetic Loci
Schizophrenia
Genes
Genome-Wide Association Study
Alleles
470 Citations

Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

Genovese, G. , Kähler, A. K. , Handsaker, R. E. , Lindberg, J. , Rose, S. A. , Bakhoum, S. F. , Chambert, K. , Mick, E. , Neale, B. M. , Fromer, M. , Purcell, S. M. , Svantesson, O. , Landén, M. , Höglund, M. , Lehmann, S. , Gabriel, S. B. , Moran, J. L. , Lander, E. S. , Sullivan, P. F. , Sklar, P. & 3 others Grönberg, H., Hultman, C. M. & McCarroll, S. A. Dec 25 2014 In : New England Journal of Medicine. 371, 26, p. 2477-2487 11 p.

Research output: Research - peer-reviewArticle

Hematopoiesis
Neoplasms
Mutation
DNA Sequence Analysis
DNA
45 Citations

Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles

Goldstein, J. I. , Fredrik Jarskog, L. , Hilliard, C. , Alfirevic, A. , Duncan, L. , Fourches, D. , Huang, H. , Lek, M. , Neale, B. M. , Ripke, S. , Shianna, K. , Szatkiewicz, J. P. , Tropsha, A. , Van Den Oord, E. J. , Cascorbi, I. , Dettling, M. , Gazit, E. , Goff, D. C. , Holden, A. L. , Kelly, D. L. & 11 others Malhotra, A. K., Nielsen, J., Pirmohamed, M., Rujescu, D., Werge, T., Levy, D. L., Josiassen, R. C., Kennedy, J. L., Lieberman, J. A., Daly, M. J. & Sullivan, P. F. Jan 1 2014 In : Nature Communications. 5, 4757

Research output: Research - peer-reviewArticle

amino acids
confidence
drugs
intervals
Agranulocytosis
32 Citations

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Rees, E. , Walters, J. T. R. , Chambert, K. D. , O'Dushlaine, C. , Szatkiewicz, J. , Richards, A. L. , Georgieva, L. , Mahoney-Davies, G. , Legge, S. E. , Moran, J. L. , Genovese, G. , Levinson, D. , Morris, D. W. , Cormican, P. , Kendler, K. S. , O'neill, F. A. , Riley, B. , Gill, M. , Corvin, A. , Sklar, P. & 9 others Hultman, C., Pato, C., Pato, M., Sullivan, P. F., Gejman, P. V., Mccarroll, S. A., O'donovan, M. C., Owen, M. J. & Kirov, G. Mar 1 2014 In : Human Molecular Genetics. 23, 6, p. 1669-1676 8 p., ddt540

Research output: Research - peer-reviewArticle

Schizophrenia
Genes
Amino Acid Transport System X-AG
Neurodevelopmental Disorders