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Aarno Palotie

Publications by Year

Research Areas

Genetic Associations and Epidemiology, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Migraine and Headache Studies

Most-Cited Works

→ Analysis of protein-coding genetic variation in 60,706 humans(2016)10,243 cited
→ Biological insights from 108 schizophrenia-associated genetic loci(2014)8,017 cited
→ Integrating common and rare genetic variation in diverse human populations(2010)3,177 cited
→ Synaptic, transcriptional and chromatin genes disrupted in autism(2014)2,891 cited
→ Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis(2011)2,712 cited
→ Identification of common genetic risk variants for autism spectrum disorder(2019)2,550 cited
→ Traumatic brain injury: integrated approaches to improve prevention, clinical care, and research(2017)

2,448 cited

→ Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism(2020)2,371 cited

→ A cross-population atlas of genetic associations for 220 human phenotypes(2021)2,288 cited

→ A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline(2012)1,712 cited