N. Freimer

N. Freimer, R. Ophoff, M. Munafo, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Integrating behavioural health tracking in human genetics research

N. Freimer, D. Mohr, 2018, Nature Reviews Genetics.

A phenome-wide examination of neural and cognitive function

Krzysztof J. Gorgolewski, Tyrone D. Cannon, N. Freimer, 2016, Scientific Data.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

P. Visscher, S. Cichon, N. Freimer, 2003, American journal of human genetics.

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

C. Spencer, K. Davis, P. Visscher, 2016, bioRxiv.

Analysis of shared heritability in common disorders of the brain

Nick C Fox, Dan J Stein, Janice M. Fullerton, 2018, Science.

Exome sequencing of Finnish isolates enhances rare-variant association power

Ira M. Hall, Thomas J. Nicholas, Thomas J Nicholas, 2019, Nature.

Mutational processes of simple-sequence repeat loci in human populations.

N. Freimer, M. Slatkin, A. Di Rienzo, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels

P. Elliott, Toshiko Tanaka, S. Bandinelli, 2011, Circulation.

Common variants associated with plasma triglycerides and risk for coronary artery disease

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2013, Nature Genetics.

Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index

Henrik, Tanya M. Teslovich, Jennie, 2012 .

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2017, bioRxiv.

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.

P. Visscher, N. Wray, E. Bramon, 2016, JAMA psychiatry.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Absolute pitch: an approach for identification of genetic and nongenetic components.

N. Freimer, S. Service, P. Johnston, 1998, American journal of human genetics.

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Bronwen L. Aken, R. Wilson, C. Sabatti, 2016, Nature Genetics.

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Christine B. Peterson, Bronwen L. Aken, R. Wilson, 2016, Nature Genetics.

Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder.

Chiara Sabatti, Paul M Thompson, Nelson B Freimer, 2015, Brain : a journal of neurology.

Self injurious behaviour in Tourette syndrome: correlates with impulsivity and impulse control

N. Freimer, D. Glidden, V. Reus, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy

Mark I. McCarthy, David Blane, Kirsi Sipilä, 2010, PLoS genetics.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population

Andres Metspalu, Mark I. McCarthy, Alex P. Reiner, 2014, PLoS genetics.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

Results of a genome-wide genetic screen for panic disorder.

S E Hodge, D F Klein, V J Vieland, 1998, American journal of medical genetics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

Chiara Sabatti, Andrew Collins, Proton Rahman, 2006, Nature Genetics.

A phenome-wide examination of neural and cognitive function

Eliza Congdon, Russell A. Poldrack, Krzysztof J. Gorgolewski, 2016 .

Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate.

Nelson B Freimer, Susan K Service, Lodewijk A Sandkuijl, 2002, American journal of human genetics.

Sex-stratified linkage analysis identifies a female-specific locus for IgE to cockroach in Costa Ricans.

N. Freimer, T. Hudson, J. Celedón, 2008, American journal of respiratory and critical care medicine.

Causes of Variation in the Static Allometry of Morphological Structures: A Case Study with Vervet Monkeys

N. Freimer, R. L. Rodríguez, T. Gaetano, 2019, Savanna Monkeys.

Population Genetic Structure of Vervet Monkeys in South Africa

N. Freimer, J. Lorenz, J. P. Grobler, 2019, Savanna Monkeys.

Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

Thomas J. Nicholas, Thomas J Nicholas, M. Pirinen, 2018 .

Future of genetics of mood disorders research

Emmanuel Mignot, Margit Burmeister, John Blangero, 2002, Biological Psychiatry.

Genome-wide association study of Tourette Syndrome

S. E. Stewart, A. Singleton, C. Sabatti, 2012, Molecular Psychiatry.

The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology

Chiara Sabatti, Nelson Freimer, C. Sabatti, 2004, Nature Genetics.

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes

N. Freimer, N. Risch, K. Giacomini, 2001, Nature Genetics.

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion.

N. Freimer, L. Pawlikowska, N. Killeen, 2004, Human molecular genetics.

Neurocognitive Phenotypes and Genetic Dissection of Disorders of Brain and Behavior

Eliza Congdon, Russell A. Poldrack, Nelson B. Freimer, 2010, Neuron.

Obesity and obesogenic growth are both highly heritable and modified by diet in a nonhuman primate model, the African green monkey (Chlorocebus aethiops sabaeus)

N. Freimer, R. Cantor, G. Weinstock, 2017, International Journal of Obesity.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations

N. Freimer, R. Ophoff, J. Molina, 2004, Psychiatric genetics.

Synaptic processes and immune-related pathways implicated in Tourette syndrome

N. Freimer, M. Nöthen, B. Leventhal, 2020, Translational Psychiatry.

Synaptic processes and immune-related pathways implicated in Tourette syndrome

N. Freimer, M. Nöthen, B. Leventhal, 2020, Translational Psychiatry.

Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder

C. Sabatti, N. Freimer, R. Cantor, 2020, Molecular Psychiatry.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Characterisation of age and polarity at onset in bipolar disorder

Till F. M. Andlauer, S. Cichon, S. Djurovic, 2021, The British Journal of Psychiatry.

Systems biology of the vervet monkey.

N. Freimer, R. Cantor, G. Weinstock, 2013, ILAR journal.

Genome‐wide association study of neurocognitive impairment and dementia in HIV‐infected adults

N. Freimer, P. Thompson, J. Becker, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Lodewijk A. Sandkuijl, M.D. (July 31, 1953–December 4, 2002).

N. Freimer, C. Wijmenga, P. Heutink, 2003 .

Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder

N. Freimer, B. Kerner, J. Deyoung, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide association study identifies eight loci associated with blood pressure

P. O’Reilly, P. Elliott, M. Jarvelin, 2009, Nature Genetics.

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

Pietro Della Briotta Parolo, Javier Gracia Tabuenca, John D. Eicher, 2019, Nature Communications.

Guidelines for association studies in Human Molecular Genetics.

C. Sabatti, N. Freimer, 2005, Human molecular genetics.

Genetics of human plasma lipidome: Understanding lipid metabolism and its link to diseases beyond traditional lipids

M. Pirinen, M. Daly, N. Freimer, 2018, bioRxiv.

Mitochondrial genome copy number in human blood-derived DNA is strongly associated with insulin levels and related metabolic traits and primarily reflects cell-type composition differences

Allison A. Regier, N. Freimer, M. Laakso, 2020, medRxiv.

The burden of deleterious variants in a non-human primate biomedical model

R. Wilson, N. Freimer, W. Warren, 2019, bioRxiv.

The Importance of the Vervet ( African Green Monkey ) as a Biomedical Model

N. Freimer, K. Dewar, L. Fairbanks, 2008 .

The enduring gap in educational attainment in schizophrenia according to the past 50 years of published research: a systematic review and meta-analysis.

N. Freimer, C. Carter, D. Barch, 2022, The lancet. Psychiatry.

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

M. Pirinen, N. Freimer, V. Salomaa, 2020, Circulation. Genomic and precision medicine.

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

M. Pirinen, N. Freimer, V. Salomaa, 2019, bioRxiv.

Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder

C. Sabatti, N. Freimer, R. Cantor, 2016, PLoS genetics.

Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents

P. Elliott, M. Jarvelin, N. Freimer, 2011, Addiction biology.

Zoonotic Potential of Simian Arteriviruses

N. Freimer, D. O’Connor, J. Rogers, 2015, Journal of Virology.

Epigenetic clock and methylation studies in vervet monkeys

S. Horvath, N. Freimer, R. Woods, 2020, GeroScience.

A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture

N. Freimer, R. Ophoff, M. Mehan, 2004, Human Genomics.

Coronary Artery Disease Risk and Lipidomic Profiles Are Similar in Hyperlipidemias With Family History and Population‐Ascertained Hyperlipidemias

M. Pirinen, N. Freimer, V. Salomaa, 2019, Journal of the American Heart Association.

Coronary artery disease risk and lipidomic profiles are similar in familial and population-ascertained hyperlipidemias

N. Freimer, V. Salomaa, A. Palotie, 2018, bioRxiv.

Correction: Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy

David M. Evans, P. O’Reilly, C. Hoggart, 2010, PLoS Genetics.

Comorbidity of bipolar disorder and substance abuse in Costa Rica: pedigree- and population-based studies.

N. Freimer, J. Molina, J. Neuhaus, 2002, Journal of affective disorders.

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Christian Gieger, Thomas Meitinger, Mario Falchi, 2009, Nature Genetics.

Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate.

Christine B. Peterson, Bronwen L. Aken, R. Wilson, 2016 .

Shifts in microbial diversity, composition, and functionality in the gut and genital microbiome during a natural SIV infection in vervet monkeys

N. Freimer, C. Apetrei, I. Pandrea, 2020, Microbiome.

Antithyroid Antibodies: Behavioral Significance

N. Freimer, V. Reus, 1990 .

ACE2 and TMPRSS2 variation in savanna monkeys (Chlorocebus spp.): Potential risk for zoonotic/anthroponotic transmission of SARS-CoV-2 and a potential model for functional studies

Christina M. Bergey, N. Freimer, V. Ramensky, 2020, PloS one.

A search for genetic loci involved in predisposition to bipolar mood disorder in the population of Antioquia, Colombia.

Reus, M. McCarthy, N. Freimer, 2000 .

Genome mapping by arbitrary amplification of yeast artificial chromosomes

N. Freimer, A. Rienzo, Soma Das, 2004, Mammalian Genome.

The effect of rare human sequence variants on the function of vesicular monoamine transporter 2.

N. Freimer, C. Glatt, J. Burman, 2004, Pharmacogenetics.

Cross-cultural Medicine Cultural Variation Nutritional and Clinical Implications

N. Freimer, N. Kretchmer, San Francisco, 2022 .

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Minna Männikkö, David Curtis, Peter Holmans, 2016, Nature Neuroscience.

Meta-analysis of genome-wide association data involving 6,100 adults of European origin identifies common variants associated with fasting glucose levels

P. Elliott, M. McCarthy, N. Freimer, 2008 .

Discovery and Refinement Supplementary

Christian Gieger, Cisca Wijmenga, Inês Barroso, 2015 .

Attitudes towards bipolar disorder and predictive genetic testing among patients and providers.

N. Freimer, V. Reus, B. Sapers, 1996, Journal of medical genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124))

P. O’Reilly, P. Elliott, L. Coin, 2011 .

Anthropogenic food enhancement alters the timing of maturational landmarks among wild savanna monkeys (Chlorocebus pygerythrus)

N. Freimer, C. Schmitt, T. Turner, 2020, bioRxiv.

Amplification with arbitrary primers.

N. Freimer, A. Di Rienzo, A. Peterson, 1996, Methods in molecular biology.

Understanding the genetic basis of mood disorders: where do we stand?

N. Freimer, V. Reus, 1997, American journal of human genetics.

Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series.

N. Freimer, Q. Duh, M. Wong, 2000, Surgery.

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.

N. Freimer, T. Gilliam, C. Kaufmann, 1989, Genomics.

Genetic Determinants of Height Growth Assessed Longitudinally from Infancy to Adulthood in the Northern Finland Birth Cohort 1966

Mark I. McCarthy, Leena Peltonen, Ioanna Tzoulaki, 2009, PLoS genetics.

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC

N. Freimer, R. Sinke, D. Barton, 1999, Human Genetics.

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC‐1] and Byler syndrome): Evidence for heterogeneity

N. Freimer, V. Carlton, K. Setchell, 1997, Hepatology.

Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q.

N. Freimer, J. Pedersen, E. Roche, 2000, American journal of human genetics.

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales

M. Jarvelin, N. Wray, T. Lehtimäki, 2012, Translational Psychiatry.

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

Nelson B. Freimer, N. Freimer, R. Houwen, 1994, Nature Genetics.

Seroprevalence of Zika Virus in Wild African Green Monkeys and Baboons

N. Freimer, D. O’Connor, J. Rogers, 2017, mSphere.

M41 IDENTIFYING NOOTROPIC DRUG TARGETS VIA LARGE-SCALE COGNITIVE GWAS AND TRANSCRIPTOMICS

Tyrone D. Cannon, I. Deary, D. Rujescu, 2019, European Neuropsychopharmacology.

Temperament Clusters in a Normal Population: Implications for Health and Disease

Eliza Congdon, Heikki Mannila, Tuija Tammelin, 2012, PloS one.

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thomas E. Nichols, Benjamin S. Aribisala, Marisa O. Hollinshead, 2014, Brain Imaging and Behavior.

Prevalence of Zika virus infection in wild African primates

N. Freimer, D. O’Connor, J. Rogers, 2016, bioRxiv.

Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids

Tanya M. Teslovich, Y. J. Kim, M. Rieder, 2010, Nature.

Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry

P. O’Reilly, P. Elliott, M. Jarvelin, 2009, Nature genetics.

Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica

N. Freimer, R. Ophoff, G. Bedoya, 2003, Human Genetics.

Local Virus Extinctions following a Host Population Bottleneck

N. Freimer, E. Delwart, A. Jasinska, 2015, Journal of Virology.

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

C. Gieger, F. Kronenberg, A. Hofman, 2011, PLoS genetics.

Mapping Correlates of Parasitism in Wild South African Vervet Monkeys (Chlorocebus aethiops)

N. Freimer, C. Schmitt, T. Turner, 2014 .

Genome-wide association study identifies multiple loci influencing human serum metabolite levels

Markus Perola, Kaisa Silander, Michael Inouye, 2012, Nature Genetics.

Molecular Population Genetics of the Northern Elephant Seal Mirounga angustirostris

N. Freimer, J. Garza, Kristy Deiner, 2017, The Journal of heredity.

Predicting Depression with Psychopathology and Temperament Traits: The Northern Finland 1966 Birth Cohort

T. Paunio, N. Freimer, M. Järvelin, 2012, Depression research and treatment.

Identifying Schizophrenia and Other Psychoses With Psychological Scales in the General Population

T. Paunio, N. Freimer, L. Peltonen, 2011, The Journal of nervous and mental disease.

Data on schizotypy and affective scales are gender and education dependent — Study in the Northern Finland 1966 Birth Cohort

T. Paunio, N. Freimer, L. Peltonen, 2010, Psychiatry Research.

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels

Gonçalo Abecasis, Michael J E Sternberg, Yun Li, 2009, Nature Genetics.

Differences in presentation and progression between severe FIC1 and BSEP deficiencies.

Richard J. Thompson, N. Freimer, L. Pawlikowska, 2010, Journal of hepatology.

Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

Dan J Stein, Melissa J. Green, Janice M. Fullerton, 2021, Nature Genetics.

Association between maternal smoking and increased symptom severity in Tourette's syndrome.

N. Freimer, V. Reus, C. Mathews, 2006, The American journal of psychiatry.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34.

C. Sabatti, N. Freimer, M. Parra, 2006, Human molecular genetics.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Dan J Stein, F. A. Schroeder, S. E. Stewart, 2014, Journal of the American Academy of Child and Adolescent Psychiatry.

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

P. O’Reilly, P. Elliott, M. Jarvelin, 2011, Proceedings of the National Academy of Sciences.

The genome-wide distribution of background linkage disequilibrium in a population isolate.

N. Freimer, R. Ophoff, S. Service, 2001, Human molecular genetics.

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

N. Freimer, S. Barondes, M. Escamilla, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population.

N. Freimer, J. Molina, M. Escamilla, 1996, American journal of medical genetics.

Mapping genes for psychiatric disorders and behavioral traits.

N. Freimer, L. McInnes, 1995, Current opinion in genetics & development.

Expanding on population studies

N. Freimer, M. Slatkin, S. Service, 1997, Nature Genetics.

Methodological issues in molecular genetic studies of mental disorders.

N. Freimer, C. Bearden, A. Jasinska, 2009, Annual review of clinical psychology.

An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees.

N. Freimer, S. Service, V. Reus, 1996, American journal of medical genetics.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Michael F. Green, Max W. Y. Lam, Catherine A. Sugar, 2022, Nature.

The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2018, bioRxiv.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2017, bioRxiv.

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

M. Jarvelin, M. Daly, K. Kristiansson, 2013, Nature Neuroscience.

Rare coding variants in ten genes confer substantial risk for schizophrenia

S. Gabriel, M. Daly, H. Kang, 2022, Nature.

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Jeffrey D. Mandell, Stephan J Sanders, N. Freimer, 2018, Cell reports.

CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

N. Freimer, E. Cook, G. Bedoya, 2013, PloS one.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

Variants in MTNR1B influence fasting glucose levels

Inês Barroso, Paul Scheet, Nicole Soranzo, 2009, Nature Genetics.

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

H. Stefánsson, N. Freimer, R. Ophoff, 2019, The American journal of psychiatry.

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Douglas W. Woods, Jae Hoon Sul, Michael S. Okun, 2016, Neuron.

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

N. Freimer, R. Ophoff, D. Clair, 2022, Nature Genetics.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

John P. Rice, Robert M. Maier, C. Spencer, 2020, Biological Psychiatry.

Genetics and Epidemiology of Tourette Syndrome

N. Freimer, D. Keen-Kim, 2006, Journal of child neurology.

Identifying Heritable Brain Phenotypes in an Extended Pedigree of Vervet Monkeys

Zhuowen Tu, Roger P Woods, Nelson B Freimer, 2009, The Journal of Neuroscience.

COMMENTARY Guidelines for association studies in Human

C. Sabatti, N. Freimer, 2005 .

False discovery rate in linkage and association genome screens for complex disorders.

Chiara Sabatti, Nelson Freimer, C. Sabatti, 2003, Genetics.

Association analysis of candidate genes for neuropsychiatric disease: the perpetual campaign.

N. Freimer, C. Glatt, 2002, Trends in genetics : TIG.

Linkage analysis of a complex pedigree with severe bipolar disorder, using a Markov chain Monte Carlo method.

C Garner, L A McInnes, S K Service, 2001, American journal of human genetics.

A fine-scale comparison of the human and chimpanzee genomes: linkage, linkage disequilibrium and sequence analysis.

N. Freimer, M. Slatkin, S. Service, 1996, Human molecular genetics.

Recombination rates in admixed individuals identified by ancestry-based inference

Ingo Ruczinski, John Novembre, Sharon L R Kardia, 2011, Nature Genetics.

Analysis of segmental duplications reveals a distinct pattern of continuation-of-synteny between human and mouse genomes

Roel A. Ophoff, Nelson B. Freimer, N. Freimer, 2007, Human Genetics.

Mismatch repair detection (MRD): high-throughput scanning for DNA variations.

N. Freimer, J. Deyoung, S. Baharloo, 2001, Human molecular genetics.

Association of Structural Variation with Cardiometabolic Traits in Finns

Ira M. Hall, Alexandra J. Scott, Allison A. Regier, 2020, bioRxiv.

Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits

R. Wilson, N. Freimer, R. Cantor, 2015, BMC Biology.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Exome Aggregation Consortium

Adam Kiezun, Sergio Islas-Andrade, Pierre Fontanillas, 2016 .

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Chiara Sabatti, Nelson B Freimer, C. Sabatti, 2006, Human molecular genetics.

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

Emily C. Hector, N. Freimer, M. Laakso, 2022, Nature Communications.

Genome-wide association study of 1,391 plasma metabolites in 6,136 Finnish men identifies 303 novel signals and provides biological insights into human diseases

Emily C. Hector, Ripatti, N. Freimer, 2021, medRxiv.

Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort

T. Paunio, N. Freimer, L. Peltonen, 2011, BMJ Open.

Phenotype mining in CNV carriers from a population cohort.

M. Jarvelin, O. Pietiläinen, T. Paunio, 2011, Human molecular genetics.

Re‐Screening serotonin receptors for genetic variants identifies population and molecular genetic complexity

N. Freimer, C. Glatt, J. Deyoung, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.

P. Visscher, N. Wray, M. Daly, 2015, International journal of epidemiology.

Understanding the Hidden Complexity of Latin American Population Isolates

C. Sabatti, N. Freimer, G. Bedoya, 2018, bioRxiv.

Immunosuppressive effect and global dysregulation of blood transcriptome in response to psychosocial stress in vervet monkeys (Chlorocebus sabaeus)

N. Freimer, J. Jentsch, G. Coppola, 2020, Scientific Reports.

Morphological variation in the genus Chlorocebus: Ecogeographic and anthropogenically mediated variation in body mass, postcranial morphology, and growth.

N. Freimer, J. Lorenz, C. Schmitt, 2018, American journal of physical anthropology.

Ancient hybridization and strong adaptation to viruses across African vervet monkey populations

R. Wilson, N. Freimer, G. Weinstock, 2016, Nature Genetics.

Anatomic Brain Asymmetry in Vervet Monkeys

Roger P. Woods, Zvart Abaryan, Matthew J. Jorgensen, 2011, PloS one.

Identification of brain transcriptional variation reproduced in peripheral blood: an approach for mapping brain expression traits

Roger P. Woods, Olivera Grujic, Matthew J. Jorgensen, 2009, Human molecular genetics.

A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus)

Thomas J. Hudson, Ken Dewar, Roel A. Ophoff, 2007, Mammalian Genome.

False Discovery Rate and Correction for Multiple Comparisons in Linkage Disequilibrium Genome Screens

C. Sabatti, N. Freimer, 2002 .

False Discovery Rate and Correction for Multiple Comparisons in Association Genome Screens for Complex Disorders

C. Sabatti, N. Freimer, S. Service, 2002 .

Variation in Scrotal Color Among Widely Distributed Vervet Monkey Populations (Chlorocebus Aethiops Pygerythrus and Chlorocebus Aethiops Sabaeus)

N. Freimer, J. Lorenz, C. Schmitt, 2013, American journal of primatology.

A non-human primate system for large-scale genetic studies of complex traits.

R. Wilson, N. Freimer, R. Cantor, 2012, Human molecular genetics.

Diversity matters: opportunities in the study of the genetics of psychotic disorders in low- and middle-income countries in Latin America

N. Freimer, N. Crossley, C. López-Jaramillo, 2020, Revista brasileira de psiquiatria.

Publisher Correction: Ancient hybridization and strong adaptation to viruses across African vervet monkey populations

R. Wilson, N. Freimer, G. Weinstock, 2018, Nature Genetics.

Factors Associated with Siman Immunodeficiency Virus Transmission in a Natural African Nonhuman Primate Host in the Wild

N. Freimer, D. Robertson, C. Apetrei, 2014, Journal of Virology.

SIVagm Infection in Wild African Green Monkeys from South Africa: Epidemiology, Natural History, and Evolutionary Considerations

N. Freimer, R. Desrosiers, D. Burke, 2013, PLoS pathogens.

Localized population divergence of vervet monkeys (Chlorocebus spp.) in South Africa: Evidence from mtDNA.

N. Freimer, J. Lorenz, C. Schmitt, 2016, American journal of physical anthropology.

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.

Shahrul Mt-Isa, Philippe Froguel, Vincent Mooser, 2009, JAMA.

Cultural variation--nutritional and clinical implications.

N. Freimer, N. Kretchmer, D. Echenberg, 1983, The Western journal of medicine.

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

Richard J. Thompson, N. Freimer, G. Mieli-Vergani, 1998, Nature Genetics.

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24.

N. Freimer, R. Thompson, S. Kocoshis, 1997, American journal of human genetics.

Replicating genotype – phenotype associations What constitutes replication of a genotype – phenotype association , and how best can it be achieved ?

Peter Donnelly, Lon R. Cardon, Ellen M. Wijsman, 2007 .

The Contribution of GWAS Loci in Familial Dyslipidemias

M. Pirinen, R. Wilson, N. Freimer, 2016, PLoS genetics.

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

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

Title CNV Analysis in Tourette Syndrome Implicates Large GenomicRearrangements in COL 8 A 1 and NRXN 1

N. Freimer, E. Cook, G. Bedoya, 2013 .

Linkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Density

C. Sabatti, N. Freimer, Yuguo Chen, 2006, Human Heredity.

Genome-Wide Linkage Scan of Bipolar Disorder in a Colombian Population Isolate Replicates Loci on Chromosomes 7p21–22, 1p31, 16p12 and 21q21–22 and Identifies a Novel Locus on Chromosome 12q

N. Freimer, M. Parra, G. Bedoya, 2010, Human Heredity.

Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.

N. Freimer, T. Gilliam, S. Warren, 1992, Genomics.

African Nonhuman Primate Host in the Wild

N. Freimer, C. Apetrei, I. Pandrea, 2014 .

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.

N. Freimer, V. Carlton, A. Knisely, 1995, Human molecular genetics.

Arteriviruses, Pegiviruses, and Lentiviruses Are Common among Wild African Monkeys

Chase W. Nelson, N. Freimer, A. Hughes, 2016, Journal of Virology.

GeneticLociAssociatedWithC-ReactiveProtein Levels and Risk of Coronary Heart Disease

Ian J. Brown, P. Elliott, L. Coin, 2017 .

Endophenotypes for psychiatric disorders: ready for primetime?

N. Freimer, C. Bearden, 2006, Trends in genetics : TIG.

A large population cohort provides normative data for investigation of temperament

N. Freimer, L. Peltonen, M. Järvelin, 2004, Acta psychiatrica Scandinavica.

Leena Peltonen-Palotie: the human side of genetics

M. McCarthy, N. Freimer, N. Schork, 2010 .

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2011, Nature Genetics.

Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica.

N. Freimer, T. Hudson, E. Silverman, 2007, Human molecular genetics.

Normal variants of Microcephalin and ASPM do not account for brain size variability.

Arthur W Toga, Roger P Woods, Nelson B Freimer, 2006, Human molecular genetics.

Cost-effective designs for linkage disequilibrium mapping of complex traits.

Nelson B Freimer, Susan K Service, Lodewijk A Sandkuijl, 2003, American journal of human genetics.

The distribution of linkage disequilibrium over anonymous genome regions.

N. Freimer, M. Slatkin, A. Chapelle, 1995, Human molecular genetics.

Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: an initial screen for bipolar disorder loci on chromosome 18.

N. Freimer, S. Barondes, J. Molina, 1999, American journal of human genetics.

Microsatellite allele frequencies in humans and chimpanzees, with implications for constraints on allele size.

N. Freimer, M. Slatkin, J. Garza, 1995, Molecular biology and evolution.

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

N. Freimer, L. Pawlikowska, R. Houwen, 1998, Nature Genetics.

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

N. Freimer, R. Ophoff, R. Baloh, 2001, American journal of human genetics.

A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis.

N. Freimer, L. Almasy, M. Escamilla, 2000, American journal of human genetics.

Characterization of expression quantitative trait loci in extensively phenotyped pedigrees ascertained for bipolar disorder

C. Sabatti, N. Freimer, Y. Benjamini, 2015, bioRxiv.

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Richard J. Thompson, N. Freimer, L. Pawlikowska, 2004, Hepatology.

The Newfoundland population: a unique resource for genetic investigation of complex diseases.

N. Freimer, B. Fernandez, P. Rahman, 2003, Human molecular genetics.

Incorrect specification of marker allele frequencies: effects on linkage analysis.

N. Freimer, S. Blower, L. Sandkuijl, 1993, American journal of human genetics.

The Genetics of Affective Disorder

N. Freimer, M. Weissman, 1990 .

Molecular Architecture and Neurobiology of Bipolar Disorder

N. Freimer, P. Zandi, C. Bearden, 2016 .

Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder

Chiara Sabatti, Nelson Freimer, Joseph DeYoung, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64

N. Freimer, T. Delhaas, R. Sinke, 1997, Human Genetics.

Characterization of Age and Polarity at Onset in Bipolar Disorder

Till F. M. Andlauer, S. Cichon, S. Djurovic, 2021, medRxiv.

Genetic mapping using haplotype and model‐free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31‐33

N. Freimer, J. Molina, S. Service, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: a follow-up study on chromosome 18.

N. Freimer, J. Molina, S. Service, 2001, American journal of medical genetics.

Compound microsatellite repeats: practical and theoretical features.

N. Freimer, C. Pabón-Peña, L. Bull, 1999, Genome research.

Fine mapping of a locus for severe bipolar mood disorder in the Costa Rican population using linkage disequilibrium methods.

Reus, N. Freimer, S. Barondes, 1997 .

DISTINCT AND SHARED CONTRIBUTIONS OF DIAGNOSIS AND SYMPTOM DOMAINS TO COGNITIVE PERFORMANCE IN SEVERE MENTAL ILLNESS

C. Sabatti, N. Freimer, R. Gur, 2019, European Neuropsychopharmacology.

Impact of temperament on depression and anxiety symptoms and depressive disorder in a population-based birth cohort.

T. Paunio, N. Freimer, L. Peltonen, 2011, Journal of Affective Disorders.

Microsatellites: evolution and mutational processes.

N. Freimer, M. Slatkin, 2007, Ciba Foundation symposium.

Prevalence and clinical correlates of explosive outbursts in Tourette Syndrome

N. Freimer, V. Reus, C. Mathews, 2013, Psychiatry Research.

Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder

C. Sabatti, N. Freimer, R. Ophoff, 2019, Psychological Medicine.

Differential impairments of episodic and working memory in schizophrenia, bipolar disorder and ADHD

Tyrone D. Cannon, Kristen M. Haut, N. Freimer, 2014 .

Transmission of Staphylococcus aureus from Humans to Green Monkeys in The Gambia as Revealed by Whole-Genome Sequencing

Harry A. Thorpe, N. Freimer, G. Weinstock, 2016, Applied and Environmental Microbiology.

Impact of the dopamine receptor gene family on temperament traits in a population‐based birth cohort

N. Freimer, L. Peltonen, M. Järvelin, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder

C. Sabatti, N. Freimer, R. Cantor, 2015, Proceedings of the National Academy of Sciences.

Tic Symptom Profiles in Subjects with Tourette Syndrome from two Genetically Isolated Populations

N. Freimer, N. Schork, V. Reus, 2007, Biological Psychiatry.

Why genetic investigation of psychiatric disorders is so difficult.

N. Freimer, C. Bearden, V. Reus, 2004, Current opinion in genetics & development.

The Human Variome Project

Sue Povey, Johan T den Dunnen, Anthony J Brookes, 2008, Science.

ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest

Jae Hoon Sul, Giovanni Coppola, Brandon Jew, 2018, bioRxiv.

Human genetics: Variants in common diseases

Chiara Sabatti, Nelson B. Freimer, C. Sabatti, 2007, Nature.

Decomposing Decision Components in the Stop-signal Task: A Model-based Approach to Individual Differences in Inhibitory Control

Russell A. Poldrack, Fred W. Sabb, Edythe D. London, 2014, Journal of Cognitive Neuroscience.

A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species

Ken Dewar, Nelson B Freimer, Rita M Cantor, 2007, Proceedings of the National Academy of Sciences.

The static allometry of sexual and non-sexual traits in vervet monkeys.

N. Freimer, C. Schmitt, T. Turner, 2015, Biological journal of the Linnean Society. Linnean Society of London.

An association study of bipolar mood disorder (type I) with the 5-HTTLPR serotonin transporter polymorphism in a human population isolate from Colombia

M. McCarthy, N. Freimer, G. Bedoya, 2000, Neuroscience Letters.

Spinal muscular atrophy is not the result of mutations at the beta‐hexosaminidase or GM2‐activator locus

N. Freimer, T. Gilliam, K. Wilhelmsen, 1991, Neurology.

Neurodegenerative disease biomarkers Aβ1–40, Aβ1–42, tau, and p‐tau181 in the vervet monkey cerebrospinal fluid: Relation to normal aging, genetic influences, and cerebral amyloid angiopathy

N. Freimer, A. Fagan, R. Woods, 2018, Brain and behavior.

Comparative developmental morphology within the genus Chlorocebus

N. Freimer, J. Lorenz, C. Schmitt, 2014 .

Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica

N. Freimer, T. Hudson, E. Silverman, 2006, Thorax.

Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

P. O’Reilly, P. Elliott, L. Coin, 2011, Proceedings of the National Academy of Sciences.

In search of a gene for hereditary cholestasis.

N. Freimer, P. Hammerman, B. Scharschmidt, 1996, Biochemical and molecular medicine.

Cultural influences on diagnosis and perception of Tourette syndrome in Costa Rica.

N. Freimer, B. V. D. van de Wetering, V. Reus, 2001, Journal of the American Academy of Child and Adolescent Psychiatry.

Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica

N. Freimer, T. Hudson, E. Silverman, 2006, Human Genetics.

Early Environment and Neurobehavioral Development Predict Adult Temperament Clusters

Eliza Congdon, Heikki Mannila, Jouni K. Seppänen, 2012, PloS one.

Roadmap for a precision-medicine initiative in the Nordic region

H. Stefánsson, N. Freimer, U. Thorsteinsdóttir, 2019, Nature Genetics.

Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

David C. Glahn, Tyler M. Moore, Raquel E. Gur, 2020, Educational and psychological measurement.

Adult age confounds estimates of static allometric slopes in a vertebrate

N. Freimer, C. Schmitt, T. Turner, 2015, Ethology, ecology & evolution.

A web-based brain atlas of the vervet monkey, Chlorocebus aethiops

Arthur W. Toga, Roger P. Woods, Matthew J. Jorgensen, 2011, NeuroImage.

Homoplasy for size at microsatellite loci in humans and chimpanzees.

N B Freimer, N. Freimer, J. Garza, 1996, Genome research.

Identification of common variants associated with human hippocampal and intracranial volumes

Marisa O. Hollinshead, Lorna M. Lopez, Thomas W. Mühleisen, 2012, Nature Genetics.

Nature Genetics Advance Online Publication Recombination Rates in Admixed Individuals Identified by Ancestry-based Inference

K. Veeramah, N. Freimer, T. Beaty, 2022 .

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

J. Danesh, M. Daly, M. Hurles, 2016, bioRxiv.

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thomas E. Nichols, Benjamin S. Aribisala, Marisa O. Hollinshead, 2014, Brain Imaging and Behavior.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Tanya M. Teslovich, P. Elliott, M. Jarvelin, 2011, Nature Genetics.

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

C. Spencer, K. Davis, P. Visscher, 2014, Nature.

Functional characterization of GATA 3 mutations causing the hypoparathyroidism-deafness-renal ( HDR ) dysplasia syndrome : insight into mechanisms of DNA binding by the GATA 3 transcription factor

N. Freimer, T. Hudson, E. Silverman, 2007 .

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.

Jeffrey D. Mandell, Stephan J Sanders, N. Freimer, 2018, Cell reports.

Costa Rica function in families of children with asthma in Genome-wide linkage analysis of pulmonary Freimer

N. Freimer, T. Hudson, E. Silverman, 2007 .

Tag SNPs chosen from HapMap perform well in several population isolates

C. Sabatti, N. Freimer, S. Service, 2007, Genetic epidemiology.

Nature Genetics Advance Online Publication Recombination Rates in Admixed Individuals Identified by Ancestry-based Inference

K. Veeramah, N. Freimer, T. Beaty, 2022 .

Structural variants in the vesicular monoamine transporter do not contribute to sporadic Parkinson's disease

N. Freimer, C. Tanner, C. Glatt, 2006, Movement disorders : official journal of the Movement Disorder Society.

Association analyses of 249 , 796 individuals reveal 18 new loci associated with body mass index

Tanya M. Teslovich, Eric, P. Elliott, 2012 .

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

Melissa J. Green, Janice M. Fullerton, Robert C. Thompson, 2019, Biological psychiatry.

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

N. Freimer, M. Nöthen, W. McMahon, 2016, Neuron.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Tanya M. Teslovich, P. Elliott, M. Jarvelin, 2010, Nature Genetics.

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.

Ian J. Brown, P. Elliott, M. Jarvelin, 2009, JAMA.

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thomas E. Nichols, Benjamin S. Aribisala, Marisa O. Hollinshead, 2014, Brain Imaging and Behavior.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.

John P. Rice, Warren W. Kretzschmar, Robert M. Maier, 2021, Biological psychiatry.

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

P. O’Reilly, P. Elliott, M. Jarvelin, 2011, Proceedings of the National Academy of Sciences.

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thomas E. Nichols, Rita Z. Goldstein, Benjamin S. Aribisala, 2014, Brain Imaging and Behavior.

Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure.

P. O’Reilly, P. Elliott, M. Jarvelin, 2009 .

Roadmap for a precision-medicine initiative in the Nordic region

Søren Brunak, Andres Metspalu, Eivind Hovig, 2019, Nature Genetics.

Mapping genes for psychiatric disorders and behavioral traits.

N. Freimer, V. Reus, L. McInnes, 1998, Current opinion in genetics & development.

The complex genetic basis of simple behavior

N. Freimer, A. Jasinska, 2009, Journal of biology.

Cost-effective designs for linkage disequilibrium mapping of complex traits.

N. Freimer, S. Service, L. Sandkuijl, 2003, American journal of human genetics.