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Biorxiv : the Preprint Server for Biology|June 12, 2025
Rapid adaptation and extinction across climates in synchronized outdoor evolution experiments of Arabidopsis thalianaXing Wu, Tatiana Bellagio, Yunru Peng, et al.Nature Computational Science|February 23, 2026
Mapping the potential and limitations of using generative AI technologies to address socio-economic challenges in LMICsRachel Adams, Fola Adeleke, Leah Junck, et al.Neurology|February 27, 2001
A randomized, controlled trial of remacemide for motor fluctuations in Parkinson's diseaseI Shoulson, J Penney, M McDermott, et al.American Journal of Epidemiology|March 24, 2023
The Environmental Influences on Child Health Outcomes (ECHO)-Wide CohortEmily A Knapp, Amii M Kress, Corette B Parker, et al.Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.Pageof 201