Christina M Hultman

发表

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.

Advancing maternal age is associated with increasing risk for autism: a review and meta-analysis.

Alexander Kolevzon, James H MacCabe, Sven Sandin, 2012, Journal of the American Academy of Child and Adolescent Psychiatry.

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

Giulio Genovese, Patrick F Sullivan, Menachem Fromer, 2016, Nature Neuroscience.

MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples.

Daniel Adkins, Patrick F Sullivan, Christina M Hultman, 2012, Epigenomics.

The Promises and Pitfalls of Genoeconomics*

Jonathan P. Beauchamp, Tamara B Harris, Magnus Johannesson, 2012, Annual review of economics.

Exome sequencing and the genetic basis of complex traits

Adam Kiezun, Patrik Magnusson, Shamil R Sunyaev, 2012, Nature Genetics.

Maternal effects for preterm birth: a genetic epidemiologic study of 630,000 families.

Yudi Pawitan, Marie Reilly, Sven Sandin, 2009, American journal of epidemiology.

Exome Aggregation Consortium

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

Recurrence risks for schizophrenia in a Swedish National Cohort

Patrick F Sullivan, Christina M Hultman, Pamela Sklar, 2006, Psychological Medicine.

Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity

Thomas Mailund, Thomas Espeseth, Patrick F Sullivan, 2016, Genetics.

Traumatic bereavement, acute dissociation, and posttraumatic stress: 14 years after the MS Estonia disaster.

Tom Lundin, Christina M Hultman, C. Hultman, 2011, Journal of traumatic stress.

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

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Preterm birth and psychiatric disorders in young adult life.

Chiara Nosarti, Larry Rifkin, James MacCabe, 2012, Archives of general psychiatry.

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

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

Covariance component models for multivariate binary traits in family data analysis

Yudi Pawitan, Christina M Hultman, Benjamin H Yip, 2008, Statistics in medicine.

Perinatal risk factors in offenders with severe personality disorder: a population-based investigation.

Martin Grann, Christina M Hultman, John R Geddes, 2012, Journal of personality disorders.

Methylome-wide association study of schizophrenia: identifying blood biomarker signatures of environmental insults.

Guimin Gao, Patrick F Sullivan, Wenan Chen, 2014, JAMA psychiatry.

Most genetic risk for autism resides with common variation

Kathryn Roeder, Ann B. Lee, Stephan Ripke, 2014, Nature Genetics.

Fetal growth restriction and schizophrenia: a Swedish twin study.

Christina M Hultman, Sven Cnattingius, C. Hultman, 2005, Twin research and human genetics : the official journal of the International Society for Twin Studies.

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

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

Estimation of SNP heritability from dense genotype data.

Stephan Ripke, Jian Yang, Peter M Visscher, 2013, American journal of human genetics.

Mental illness, suicide and creativity: 40-year prospective total population study.

Niklas Långström, Christina M Hultman, Mikael Landén, 2013, Journal of psychiatric research.

Parental Psychiatric Disorders Associated With Autism Spectrum Disorders in the Offspring

Maria Feychting, David A Savitz, Christina M Hultman, 2008, Pediatrics.