Query author contributions in Reactome

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Details on Person Lifton, Richard P

Class:Id	Person:6797770
_displayName	Lifton, Richard P
_timestamp	2015-09-16 10:26:39
created	[InstanceEdit:6797849] Garapati, Phani Vijay, 2015-09-16
firstname	Richard P
initial	RP
surname	Lifton
(author)	[LiteratureReference:6797896] Sequence variants in SLITRK1 are associated with Tourette's syndrome [LiteratureReference:6802011] Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas [LiteratureReference:9652716] Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma [LiteratureReference:9677799] An SGK1 site in WNK4 regulates Na+ channel and K+ channel activity and has implications for aldosterone signaling and K+ homeostasis [LiteratureReference:9698138] The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities [LiteratureReference:9755840] X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19 [LiteratureReference:9843011] Mutations in KDSR Cause Recessive Progressive Symmetric Erythrokeratoderma [LiteratureReference:9856303] ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption [LiteratureReference:9922683] CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation
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No pathways have been reviewed or authored by Lifton, Richard P (6797770)