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Nature Communications|December 1, 2020
muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics dataHelena L Crowell, Charlotte Soneson, Pierre-Luc Germain, et al.
Cell|December 25, 2012
Whole-genome sequencing in autism identifies hot spots for de novo germline mutationJacob J Michaelson, Yujian Shi, Madhusudan Gujral, et al.
European Journal of Human Genetics : EJHG|January 5, 2006
Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian populationDheeraj Malhotra, Katayoon Darvishi, Manmohan Lohra, et al.
Life Science Alliance|March 24, 2021
CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq dataAlmut Lütge, Joanna Zyprych-Walczak, Urszula Brykczynska Kunzmann, et al.
Human Genetics|September 16, 2005
IL-10 promoter single nucleotide polymorphisms are significantly associated with resistance to leprosyDheeraj Malhotra, Katayoon Darvishi, Soni Sood, et al.
Neuron|December 27, 2011
High frequencies of de novo CNVs in bipolar disorder and schizophreniaDheeraj Malhotra, Shane McCarthy, Jacob J Michaelson, et al.
Plos Computational Biology|June 15, 2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genomeKymberleigh A Pagel, Danny Antaki, AoJie Lian, et al.
Biological Psychiatry|November 14, 2017
Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem CellsFabiele Baldino Russo, Beatriz Camille Freitas, Graciela Conceição Pignatari, et al.
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