User profiles for C. M. Hultman

Christina Hultman

Karolinska INstitutet
Verified email at ki.se
Cited by 84610

Exome sequencing and the genetic basis of complex traits

…, P Sklar, PF Sullivan, JL Moran, CM Hultman… - Nature …, 2012 - nature.com
Shamil Sunyaev and colleagues present exome sequencing methods and their applications
in studies to identify the genetic basis of human complex traits. They include analyses of the …

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

S Sandin, CM Hultman, A Kolevzon, R Gross… - Journal of the American …, 2012 - Elsevier
OBJECTIVE: We conducted a meta-analysis of epidemiological studies investigating the
association between maternal age and autism. METHOD: Using recommended guidelines for …

The promises and pitfalls of genoeconomics

…, A Grankvist, CM Hultman… - Annu. Rev …, 2012 - annualreviews.org
This article reviews existing research at the intersection of genetics and economics, presents
some new findings that illustrate the state of genoeconomics research, and surveys the …

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

…, A Corvin, NJ Craddock, M Gill, CM Hultman… - Nature, 2009 - nature.com
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by
hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80% 1 , 2 . …

Synaptic, transcriptional and chromatin genes disrupted in autism

…, EH Cook, CM Freitag, M Gill, CM Hultman… - Nature, 2014 - nature.com
The genetic architecture of autism spectrum disorder involves the interplay of common and
rare variants and their impact on hundreds of genes. Using exome sequencing, here we …

[HTML][HTML] Analysis of protein-coding genetic variation in 60,706 humans

…, JC Florez, SB Gabriel, G Getz, SJ Glatt, CM Hultman… - Nature, 2016 - nature.com
Large-scale reference data sets of human genetic variation are critical for the medical and
functional interpretation of DNA sequence changes. Here we describe the aggregation and …

Biological insights from 108 schizophrenia-associated genetic loci

…, T Esko, PV Gejman, M Gill, H Gurling, CM Hultman… - Nature, 2014 - nature.com
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

[HTML][HTML] Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

…, P Sklar, H Grönberg, CM Hultman… - … England Journal of …, 2014 - Mass Medical Soc
Background Cancers arise from multiple acquired mutations, which presumably occur over
many years. Early stages in cancer development might be present years before cancers …

[PDF][PDF] Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

…, I Hertz-Picciotto, DM Hougaard, CM Hultman… - Cell, 2020 - cell.com
We present the largest exome sequencing study of autism spectrum disorder (ASD) to date (n
= 35,584 total samples, 11,986 with ASD). Using an enhanced analytical framework to …

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

…, Y Pawitan, TD Cannon, PF Sullivan, CM Hultman - The Lancet, 2009 - thelancet.com
Background Whether schizophrenia and bipolar disorder are the clinical outcomes of discrete
or shared causative processes is much debated in psychiatry. We aimed to assess genetic …