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Nature Human Behaviour|April 17, 2019
Imprint of assortative mating on the human genomeLoic Yengo, Matthew R Robinson, Matthew C Keller, et al.
Genetics|May 2, 2019
Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model TraitV Kartik Chundru, Riccardo E Marioni, James G D Prendergast, et al.
BMC Pediatrics|August 29, 2018
Study protocol for the Australian autism biobank: an international resource to advance autism discovery researchGail A Alvares, Paul A Dawson, Cheryl Dissanayake, et al.
BMJ Open|February 26, 2022
Australian Parkinson's Genetics Study (APGS): pilot (n=1532)Svetlana Bivol, George D Mellick, Jacob Gratten, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohortFleur C Garton, Beben Benyamin, Qiongyi Zhao, et al.
JAMA Psychiatry|July 4, 2019
Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association StudySathish Periyasamy, Sujit John, Raman Padmavati, et al.
Nature Communications|March 8, 2020
Analysis of DNA methylation associates the cystine-glutamate antiporter SLC7A11 with risk of Parkinson's diseaseCostanza L Vallerga, Futao Zhang, Javed Fowdar, et al.
Molecular Autism|February 11, 2021
Analysis of common genetic variation and rare CNVs in the Australian Autism BiobankChloe X Yap, Gail A Alvares, Anjali K Henders, et al.
Genome Medicine|August 25, 2019
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageingQian Zhang, Costanza L Vallerga, Rosie M Walker, et al.
Genome Medicine|November 19, 2017
Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in ChineseJacob Gratten, Qiongyi Zhao, Beben Benyamin, et al.
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