Binita M. Kamath - Concepedia

Author

Binita M. Kamath

Also Known As

B Kamath, B M KAMATH, B M Kamath, B. Kamath, B.M. Kamath, BINITA M. KAMATH, Binita Kamath, Binita M Kamath, Binita M. Kamath, Binita Maya Kamath

267

Publications

8.7K

Citations

H-Index

129

Concepts

All Affiliations

Hospital for Sick Children University of Toronto Children's Hospital of Philadelphia SickKids Foundation University of Colorado Denver

About

Binita M. Kamath is an author at Hospital for Sick Children specializing in medicine, pathology, and hepatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	36	2.8K
2	Health Sciences	6	6	304
3	Allergy	3	3	207
4	Education	2	2	181
5	Engineering	2	2	65

Binita M. Kamath

101

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Directed differentiation of cholangiocytes from human pluripotent stem cells Mina Ogawa, Shinichiro Ogawa, Christine E. Bear, Nature Biotechnology Induced Pluripotent Stem CellDevelopmental BiologyDirected DifferentiationMedicineStem Cell Research	2015	303
Mutations in TJP2 cause progressive cholestatic liver disease Melissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, Nature Genetics HepatologyBiliary TractLiver PhysiologyPathologyHepatology Inflammation	2014	288
Frailty in liver transplantation: An expert opinion statement from the American Society of Transplantation Liver and Intestinal Community of Practice Jennifer C. Lai, Christopher J. Sonnenday, Elliot B. Tapper, American Journal of Transplantation	2019	261
<i>NOTCH2</i> mutations in Alagille syndrome Binita M. Kamath, Robert C. Bauer, Kathleen M. Loomes, Journal of Medical Genetics	2011	214
The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration Mark Deneau, Wael El‐Matary, Pamela L. Valentino, Hepatology	2017	214
Consequences of <i>JAG1</i> mutations Binita M. Kamath Journal of Medical Genetics	2003	186
Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference Lisa M. Guay‐Woodford, John J. Bissler, Michael Braun, The Journal of Pediatrics GlomerulonephritisUrologyRenal DiseaseMedicineKidney Failure	2014	176
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial Richard J. Thompson, Henrik Arnell, Reha Artan, The Lancet. Gastroenterology & hepatology	2022	157
Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia Benjamin L. Shneider, John C. Magee, Saul J. Karpen, The Journal of Pediatrics UrologyHepatologyBiliary TractLiver PhysiologyPathology	2015	137
Alagille syndrome mutation update: Comprehensive overview of<i>JAG1</i>and<i>NOTCH2</i>mutation frequencies and insight into missense variant classification Melissa A. Gilbert, Robert C. Bauer, Ramakrishnan Rajagopalan, Human Mutation Family MembersGeneticsImmunodeficienciesGenetic EpidemiologyImmunology	2019	137

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