Publications:

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Genetic variation in human drug-related genes.

Genome Medicine

Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS

Publication Date: 2017-12-22

Variant appearance in text: rs367897068

PubMed Link: 29273096

Variant Present in the following documents:

• 13073_2017_502_MOESM2_ESM.xlsx, sheet 2

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Characterization of ADME gene variation in 21 populations by exome sequencing.

Pharmacogenetics And Genomics

Hovelson, Daniel H DH; Xue, Zhengyu Z; Zawistowski, Matthew M; Ehm, Margaret G MG; Harris, Elizabeth C EC; Stocker, Sophie L SL; Gross, Annette S AS; Jang, In-Jin IJ; Ieiri, Ichiro I; Lee, Jong-Eun JE; Cardon, Lon R LR; Chissoe, Stephanie L SL; Abecasis, Gonçalo G; Nelson, Matthew R MR

Publication Date: 2017-03

Variant appearance in text: rs367897068

PubMed Link: 27984508

Variant Present in the following documents:

• fpc-27-089-s005.xlsx, sheet 2

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Characterization of clinical and genetic risk factors associated with dyslipidemia after kidney transplantation.

Disease Markers

Numakura, Kazuyuki K; Kagaya, Hideaki H; Yamamoto, Ryohei R; Komine, Naoki N; Saito, Mitsuru M; Hiroshi, Tsuruta T; Akihama, Susumu S; Inoue, Takamitsu T; Narita, Shintaro S; Tsuchiya, Norihiko N; Habuchi, Tomonori T; Niioka, Takenori T; Miura, Masatomo M; Satoh, Shigeru S

Publication Date: 2015

Variant appearance in text: UGT1A6: G394A

PubMed Link: 25944971

Variant Present in the following documents:

• Main text

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Polymorphisms in heterocyclic aromatic amines metabolism-related genes are associated with colorectal adenoma risk.

International Journal Of Molecular Epidemiology And Genetics

Eichholzer, Monika M; Rohrmann, Sabine S; Barbir, Aline A; Hermann, Silke S; Teucher, Birgit B; Kaaks, Rudolf R; Linseisen, Jakob J

Publication Date: 2012

Variant appearance in text: UGT1A7: G392A

PubMed Link: 22724046

Variant Present in the following documents:

• Main text

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Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects.

Birth Defects Research. Part C, Embryo Today : Reviews

Shi, Min M; Wehby, George L GL; Murray, Jeffrey C JC

Publication Date: 2008-03

Variant appearance in text: UGT1A7: G392A

PubMed Link: 18383123

Variant Present in the following documents:

• Main text

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Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants.

American Journal Of Human Genetics

Shi, Min M; Christensen, Kaare K; Weinberg, Clarice R CR; Romitti, Paul P; Bathum, Lise L; Lozada, Anthony A; Morris, Richard W RW; Lovett, Michael M; Murray, Jeffrey C JC

Publication Date: 2007-01

Variant appearance in text: UGT1A7: G392A

PubMed Link: 17160896

Variant Present in the following documents:

• Main text

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Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.

World Journal Of Gastroenterology

Machida, Haruhisa H; Tsukamoto, Kazuhiro K; Wen, Chun-Yang CY; Shikuwa, Saburou S; Isomoto, Hajime H; Mizuta, Yohei Y; Takeshima, Fuminao F; Murase, Kunihiko K; Matsumoto, Naomichi N; Murata, Ikuo I; Kohno, Shigeru S; Wen, Chen-Yang CY

Publication Date: 2005-08-21

Variant appearance in text: UGT1A7: G392A

PubMed Link: 16097053

Variant Present in the following documents:

• Main text

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Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients.

Japanese Journal Of Cancer Research : Gann

Ando, Maki M; Ando, Yuichi Y; Sekido, Yoshitaka Y; Ando, Masahiko M; Shimokata, Kaoru K; Hasegawa, Yoshinori Y

Publication Date: 2002-05

Variant appearance in text: UGT1A7: G392A

PubMed Link: 12036456

Variant Present in the following documents:

• CAS-93-591.pdf

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