Works matching IS 03406717 AND DT 2014 AND VI 133 AND IP 7

Results: 10

The impact of microRNA expression on cellular proliferation.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 931, doi. 10.1007/s00439-014-1434-4
By:
- Lenkala, Divya;
- LaCroix, Bonnie;
- Gamazon, Eric;
- Geeleher, Paul;
- Im, Hae;
- Huang, R.
Publication type:
Article
CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in Vietnam.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 883, doi. 10.1007/s00439-014-1430-8
By:
- Grant, Audrey;
- Cobat, Aurelie;
- Thuc, Nguyen;
- Orlova, Marianna;
- Huong, Nguyen;
- Gaschignard, Jean;
- Alter, Andrea;
- Ba, Nguyen;
- Thai, Vu;
- Abel, Laurent;
- Alcaïs, Alexandre;
- Schurr, Erwin
Publication type:
Article
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 869, doi. 10.1007/s00439-014-1427-3
By:
- Eicher, John;
- Powers, Natalie;
- Miller, Laura;
- Mueller, Kathryn;
- Mascheretti, Sara;
- Marino, Cecilia;
- Willcutt, Erik;
- DeFries, John;
- Olson, Richard;
- Smith, Shelley;
- Pennington, Bruce;
- Tomblin, J.;
- Ring, Susan;
- Gruen, Jeffrey
Publication type:
Article
Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 939, doi. 10.1007/s00439-014-1436-2
By:
- Basel-Vanagaite, Lina;
- Yilmaz, Rüstem;
- Tang, Sha;
- Reuter, Miriam;
- Rahner, Nils;
- Grange, Dorothy;
- Mortenson, Megan;
- Koty, Patrick;
- Feenstra, Heather;
- Farwell Gonzalez, Kelly;
- Sticht, Heinrich;
- Boddaert, Nathalie;
- Désir, Julie;
- Anyane-Yeboa, Kwame;
- Zweier, Christiane;
- Reis, André;
- Kubisch, Christian;
- Jewett, Tamison;
- Zeng, Wenqi;
- Borck, Guntram
Publication type:
Article
Association and interaction analyses of 5-HT3 receptor and serotonin transporter genes with alcohol, cocaine, and nicotine dependence using the SAGE data.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 905, doi. 10.1007/s00439-014-1431-7
By:
- Yang, Jiekun;
- Li, Ming
Publication type:
Article
Characterization of mitochondrial haplogroups in a large population-based sample from the United States.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 861, doi. 10.1007/s00439-014-1421-9
By:
- Mitchell, Sabrina;
- Goodloe, Robert;
- Brown-Gentry, Kristin;
- Pendergrass, Sarah;
- Murdock, Deborah;
- Crawford, Dana
Publication type:
Article
Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 847, doi. 10.1007/s00439-014-1423-7
By:
- Sarasua, Sara;
- Boccuto, Luigi;
- Sharp, Julia;
- Dwivedi, Alka;
- Chen, Chin-Fu;
- Rollins, Jonathan;
- Rogers, R.;
- Phelan, Katy;
- DuPont, Barbara
Publication type:
Article
A human rights approach to an international code of conduct for genomic and clinical data sharing.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 895, doi. 10.1007/s00439-014-1432-6
By:
- Knoppers, Bartha;
- Harris, Jennifer;
- Budin-Ljøsne, Isabelle;
- Dove, Edward
Publication type:
Article
Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 919, doi. 10.1007/s00439-014-1435-3
By:
- An, Ping;
- Straka, Robert;
- Pollin, Toni;
- Feitosa, Mary;
- Wojczynski, Mary;
- Daw, E.;
- O'Connell, Jeffrey;
- Gibson, Quince;
- Ryan, Kathleen;
- Hopkins, Paul;
- Tsai, Michael;
- Lai, Chao-Qiang;
- Province, Michael;
- Ordovas, Jose;
- Shuldiner, Alan;
- Arnett, Donna;
- Borecki, Ingrid
Publication type:
Article
Disruption of long-range gene regulation in human genetic disease: a kaleidoscope of general principles, diverse mechanisms and unique phenotypic consequences.
Published in:
Human Genetics, 2014, v. 133, n. 7, p. 815, doi. 10.1007/s00439-014-1424-6
By:
- Bhatia, Shipra;
- Kleinjan, Dirk
Publication type:
Article