Reactome: A Curated Pathway Database

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Pathways reviewed by Shukla, Suneet (6797618)

DB_ID Name
5619084 ABC transporter disorders
5679090 Defective ABCG8 causes gallbladder disease 4 and sitosterolemia
5679096 Defective ABCG5 causes sitosterolemia
5679001 Defective ABCC2 causes Dubin-Johnson syndrome
5682113 Defective ABCA1 causes Tangier disease
5682294 Defective ABCA12 causes autosomal recessive congenital ichthyosis type 4B
5683177 Defective ABCC8 can cause hypoglycemias and hyperglycemias
5683329 Defective ABCD4 causes methylmalonic aciduria and homocystinuria, cblj type (MAHCJ)
5683678 Defective ABCA3 causes pulmonary surfactant metabolism dysfunction type 3 (SMDP3)
5684045 Defective ABCD1 causes adrenoleukodystrophy (ALD)
5690338 Defective ABCC6 causes pseudoxanthoma elasticum (PXE)

Details on Person Shukla, Suneet

Class:IdPerson:6797618
_displayNameShukla, Suneet
_timestamp2017-08-22 20:43:08
created[InstanceEdit:6797620] Jassal, Bijay, 2015-09-15
firstnameSuneet
initialS
surnameShukla
(author)[InstanceEdit:6797619] Shukla, Suneet, 2015-09-15
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