about
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis.Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition.Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies.Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics.meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysFrom genetics to physiology at lastNatural Selection Shapes Codon Usage in the Human Genome
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Q36686140-B00F8E05-FC0B-44F6-A0BB-5AE82E31A019Q36766098-923DC9F0-DCAD-4C66-9C1D-E87AC921B691Q36851455-B92E854A-C5CD-4F6F-8D1C-9868FB24D9F6Q38576243-DB3B797D-A965-4CDC-9880-44957B0B3FC7Q41349016-B97081B6-DC0E-44FB-8A3C-66CAB0E8A34DQ57061664-EFB2390E-76AF-4378-AE13-C7B154D514FFQ59096558-C2C63945-937A-4654-88CD-6BAA193441A7Q96224430-ACDB724C-9DE1-4AFF-B53C-EB8E55D05076
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description
investigador
@es
researcher
@en
name
Ryan S Dhindsa
@en
type
label
Ryan S Dhindsa
@en
prefLabel
Ryan S Dhindsa
@en
P31
P496
0000-0002-8965-0813