N. Freimer

B. Kerner, N. Freimer, Diana L. Brugman, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic association signal near NTN4 in Tourette syndrome

P. Paschou, E. Gamazon, Y. Worbe, 2014, Annals of neurology.

Insight into bile duct differentiation takes (notched) wings

A. Knisely, N. Freimer, 1998, Hepatology.

A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees

C. Sabatti, M. Parra, G. Bedoya, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population

J. Molina, S. Lewitzky, S. Jawahar, 2001, Proceedings of the National Academy of Sciences of the United States of America.

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

Kristen K. Dang, D. A. Lewis, C. Spencer, 2019, Nature Genetics.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Hailiang Huang, Chiara Sabatti, Kevin Eggan, 2017, bioRxiv.

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

H. Stefánsson, B. Leventhal, W. McMahon, 2023, Biological Psychiatry.

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

R. Wilson, R. Cantor, G. Weinstock, 2015, BMC Biology.

of Virus in Wild African Green Monkeys and Baboons.

J. Rogers, A. Bailey, T. Friedrich, 2017 .

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

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

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Sara B. Linker, Evan Z. Macosko, Thomas G. Gilgenast, 2023, Cell genomics.

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

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

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.

Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

John P. Rice, Melissa J. Green, Janice M. Fullerton, 2020, medRxiv.

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.

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.

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

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

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

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

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Han Xu, Stephan Ripke, Chongzhi Zang, 2014, American journal of human genetics.

Allele frequencies at microsatellite loci: the stepwise mutation model revisited.

N. Freimer, M. Slatkin, A. Valdés, 1993, Genetics.

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 phenome-wide examination of neural and cognitive function

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

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.

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.

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

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

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.

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.

Mapping the human genetic architecture of COVID-19

Mattia G. Bergomi, Christopher M. DeBoever, Matthew A. Wiles, 2021, Nature.

Expanding the range of ZNF804A variants conferring risk of psychosis

R A Ophoff, T Sigmundsson, Pall I. Olason, 2011, Molecular Psychiatry.

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.

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.

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

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

Age at first birth in women is genetically associated with increased risk of schizophrenia

Hoffmann, Hartmann, Roussos, 2017, Scientific Reports.

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

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

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.

Schizophrenia genetic variants are not associated with intelligence

A F Terwisscha van Scheltinga, S C Bakker, N E M van Haren, 2013, Psychological Medicine.

Cognitive ontologies for neuropsychiatric phenomics research

D. S. Parker, N. Freimer, R. Poldrack, 2009, Cognitive neuropsychiatry.

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.

Country-level gender inequality is associated with structural differences in the brains of women and men

Juan P. Ramirez-Mahaluf, Tiffany M Chaim-Avancini, A. Compte, 2023, Proceedings of the National Academy of Sciences of the United States of America.

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.

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.

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

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

Homoplasy for size at microsatellite loci in humans and chimpanzees.

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

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

N. Wray, H. Stefánsson, D. Rujescu, 2019, Nature Genetics.

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

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

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

P. Visscher, J. Sebat, D. Malhotra, 2016, Nature Genetics.

Genetic association signal near NTN4 in Tourette syndrome

P. Paschou, E. Gamazon, Y. Worbe, 2014, Annals of neurology.

Schizophrenia genetic variants are not associated with intelligence

P. Donnelly, P. Visscher, H. Stefánsson, 2013, Psychological Medicine.

Geospatial analysis reveals distinct hotspots of severe mental illness

C. Sabatti, R. Gur, T. Teshiba, 2022, medRxiv.

Distinct and shared contributions of diagnosis and symptom domains to cognitive performance in severe mental illness in the Paisa population: a case-control study.

T. Teshiba, S. Service, M. C. López, 2020, The lancet. Psychiatry.

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.

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

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

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

Tanya M. Teslovich, M. Jarvelin, L. Coin, 2010, Nature genetics.

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.

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

P. Visscher, E. Bramon, S. Djurovic, 2016, JAMA psychiatry.

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.

Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations.

N. Freimer, S. Service, D. Lang, 1999, American journal of human genetics.

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

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

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.

A large population cohort provides normative data for investigation of temperament

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

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

M. Pirinen, C. Freeman, P. Deloukas, 2020 .

The genome of the vervet ( Chlorocebus aethiops sabaeus )

Matthew W. Hahn, Bronwen L. Aken, T. Graves, 2016 .

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.