Slco1b1 Genotype
SLCO1B1 Genotype is a genetic polymorphism of the solute carrier organic anion transporter family member 1B1 gene that influences hepatic uptake of drugs and is associated with interindividual variability in pharmacokinetics and drug response in pediatric populations.
240
Publications
17.5K
Citations
1.7K
Authors
568
Institutions
Publications per year
2017–2026
73
Parents
240
1–5 of 240
1.7K
27
h-index
16
h-index
11
h-index
9
h-index
Cincinnati Children's Hospital Medical Center, United States
7 publications · 1.4K citations
7
h-index
1–5 of 1.7K
568

University of Helsinki
Helsinki, Finland
26 h-index
121 publications
16.7K citations

Helsinki University Hospital
Helsinki, Finland
24 h-index
99 publications
16.1K citations

Central South University
Changsha, China
13 h-index
112 publications
5.5K citations
PharmacoGenetics (China)
Hong Kong, China
12 h-index
108 publications
7.6K citations

St. Jude Children's Research Hospital
Memphis, United States
8 h-index
45 publications
9.8K citations

University of Liverpool
Liverpool, United Kingdom
8 h-index
34 publications
1.8K citations
Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology
Stuttgart, Germany
8 h-index
37 publications
6.7K citations
Duke University
Durham, United States
7 h-index
17 publications
2K citations
1–8 of 568
27 publications · 2.8K citations
24
h-index
CPT · 20 publications · 3.6K citations
20
h-index
15 publications · 891 citations
15
h-index
20 publications · 673 citations
14
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BJCP · 8 publications · 494 citations
8
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1–5