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Works matching IS 00034800 AND DT 2016 AND VI 80 AND IP 6

Results: 6

1

Glucuronic Acid Epimerase (GLCE) Variant rs3865014 (A>G) Is Associated with BMI, Blood Hemoglobin, Hypertension, and Cerebrovascular Events, the TAMRISK Study.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 332, doi. 10.1111/ahg.12166

By:

Kunnas, Tarja;
Solakivi, Tiina;
Määttä, Kirsi;
Nikkari, Seppo T.

Publication type:

Article

2

In Vitro Functional Analyses of Infrequent Nucleotide Variants in the Lactase Enhancer Reveal Different Molecular Routes to Increased Lactase Promoter Activity and Lactase Persistence.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 307, doi. 10.1111/ahg.12167

By:

Liebert, Anke;
Jones, Bryony L.;
Danielsen, Erik Thomas;
Olsen, Anders Krüger;
Swallow, Dallas M.;
Troelsen, Jesper T.

Publication type:

Article

3

Association of rs11643718 SLC12A3 and rs741301 ELMO1 Variants with Diabetic Nephropathy in South Indian Population.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 336, doi. 10.1111/ahg.12174

By:

Bodhini, Dhanasekaran;
Chidambaram, Manickam;
Liju, Samuel;
Revathi, Balakannan;
Laasya, Dhandapani;
Sathish, Natarajan;
Kanthimathi, Sekar;
Ghosh, Saurabh;
Anjana, Ranjit Mohan;
Mohan, Viswanathan;
Radha, Venkatesan

Publication type:

Article

4

MICA Gene Deletion in 3411 DNA Samples from Five Distinct Populations in Mainland China and Lack of Association with Nasopharyngeal Carcinoma (NPC) in a Southern Chinese Han population.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 319, doi. 10.1111/ahg.12175

By:

Wang, WenYi;
Tian, Wei;
Zhu, FaMing;
Li, LiXin;
Cai, JinHong;
Wang, Fan;
Liu, KangLong;
Jin, HeKun;
Wang, JunLong

Publication type:

Article

5

The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 342, doi. 10.1111/ahg.12176

By:

Khan, Muzammil Ahmad;
Khan, Saadullah;
Windpassinger, Christian;
Badar, Muhammad;
Nawaz, Zafar;
Mohammad, Ramzi M

Publication type:

Article

6

Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.

Published in:

Annals of Human Genetics, 2016, v. 80, n. 6, p. 327, doi. 10.1111/ahg.12177

By:

Manzoli, Gabrielle N.;
Bademci, Guney;
Acosta, Angelina X.;
Félix, Têmis M.;
Cengiz, F.Basak;
Foster, Joseph;
Da Silva, Danniel S. Dias;
Menendez, Ibis;
Sanchez‐Pena, Isalis;
Tekin, Demet;
Blanton, Susan H.;
Abe‐Sandes, Kiyoko;
Liu, Xue Zhong;
Tekin, Mustafa

Publication type:

Article