Works matching IS 03406717 AND DT 2016 AND VI 135 AND IP 8

Results: 13

Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 869, doi. 10.1007/s00439-016-1680-8
By:
- Sajuthi, Satria;
- Sharma, Neeraj;
- Chou, Jeff;
- Palmer, Nicholette;
- McWilliams, David;
- Beal, John;
- Comeau, Mary;
- Ma, Lijun;
- Calles-Escandon, Jorge;
- Demons, Jamehl;
- Rogers, Samantha;
- Cherry, Kristina;
- Menon, Lata;
- Kouba, Ethel;
- Davis, Donna;
- Burris, Marcie;
- Byerly, Sara;
- Ng, Maggie;
- Maruthur, Nisa;
- Patel, Sanjay
Publication type:
Article
The hnRNP family: insights into their role in health and disease.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 851, doi. 10.1007/s00439-016-1683-5
By:
- Geuens, Thomas;
- Bouhy, Delphine;
- Timmerman, Vincent
Publication type:
Article
IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 881, doi. 10.1007/s00439-016-1684-4
By:
- Furlan, Larissa;
- Marson, Fernando;
- Ribeiro, José;
- Bertuzzo, Carmen;
- Salomão Junior, João;
- Souza, Dorotéia
Publication type:
Article
De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 909, doi. 10.1007/s00439-016-1685-3
By:
- Long, Pamela;
- Zimmermann, Michael;
- Kim, Maengjo;
- Evans, Jared;
- Xu, Xiaolei;
- Olson, Timothy
Publication type:
Article
Epigenetic and genetic variation in GATA5 is associated with gastric disease risk.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 895, doi. 10.1007/s00439-016-1687-1
By:
- Sobota, Rafal;
- Kodaman, Nuri;
- Mera, Robertino;
- Piazuelo, M.;
- Bravo, Luis;
- Pazos, Alvaro;
- Zabaleta, Jovanny;
- Delgado, Alberto;
- El-Rifai, Wael;
- Morgan, Douglas;
- Wilson, Keith;
- Correa, Pelayo;
- Williams, Scott;
- Schneider, Barbara
Publication type:
Article
Identification of a homozygous nonsense mutation in KIAA0556 in a consanguineous family displaying Joubert syndrome.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 919, doi. 10.1007/s00439-016-1689-z
By:
- Roosing, Susanne;
- Rosti, Rasim;
- Rosti, Basak;
- Vrieze, Erik;
- Silhavy, Jennifer;
- Wijk, Erwin;
- Wakeling, Emma;
- Gleeson, Joseph
Publication type:
Article
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 923, doi. 10.1007/s00439-016-1690-6
By:
- Teerlink, Craig;
- Leongamornlert, Daniel;
- Dadaev, Tokhir;
- Thomas, Alun;
- Farnham, James;
- Stephenson, Robert;
- Riska, Shaun;
- McDonnell, Shannon;
- Schaid, Daniel;
- Catalona, William;
- Zheng, S.;
- Cooney, Kathleen;
- Ray, Anna;
- Zuhlke, Kimberly;
- Lange, Ethan;
- Giles, Graham;
- Southey, Melissa;
- Fitzgerald, Liesel;
- Rinckleb, Antje;
- Luedeke, Manuel
Publication type:
Article
Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
Published in:
2016
By:
- Brenner, Darren;
- Brennan, Paul;
- Boffetta, Paolo;
- Amos, Christopher;
- Spitz, Margaret;
- Chen, Chu;
- Goodman, Gary;
- Heinrich, Joachim;
- Bickeböller, Heike;
- Rosenberger, Albert;
- Risch, Angela;
- Muley, Thomas;
- McLaughlin, John;
- Benhamou, Simone;
- Bouchardy, Christine;
- Lewinger, Juan;
- Witte, John;
- Chen, Gary;
- Bull, Shelley;
- Hung, Rayjean
Publication type:
Erratum
Differential frequency of NKG2C/ KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 939, doi. 10.1007/s00439-016-1694-2
By:
- Goncalves, Adriana;
- Makalo, Pateh;
- Joof, Hassan;
- Burr, Sarah;
- Ramadhani, Athumani;
- Massae, Patrick;
- Malisa, Aiweda;
- Mtuy, Tara;
- Derrick, Tamsyn;
- Last, Anna;
- Nabicassa, Meno;
- Cassama, Eunice;
- Houghton, Joanna;
- Palmer, Christine;
- Pickering, Harry;
- Burton, Matthew;
- Mabey, David;
- Bailey, Robin;
- Goodier, Martin;
- Holland, Martin
Publication type:
Article
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.
Published in:
2016
By:
- Pourcain, Beate;
- Haworth, C.;
- Davis, O.;
- Wang, Kai;
- Timpson, Nicholas;
- Evans, David;
- Kemp, John;
- Ronald, Angelica;
- Price, Tom;
- Meaburn, Emma;
- Ring, Susan;
- Golding, Jean;
- Hakonarson, Hakon;
- Plomin, R.;
- Smith, George
Publication type:
Erratum
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 953, doi. 10.1007/s00439-016-1697-z
By:
- Yan, Denise;
- Tekin, Demet;
- Bademci, Guney;
- Foster, Joseph;
- Cengiz, F.;
- Kannan-Sundhari, Abhiraami;
- Guo, Shengru;
- Mittal, Rahul;
- Zou, Bing;
- Grati, Mhamed;
- Kabahuma, Rosemary;
- Kameswaran, Mohan;
- Lasisi, Taye;
- Adedeji, Waheed;
- Lasisi, Akeem;
- Menendez, Ibis;
- Herrera, Marianna;
- Carranza, Claudia;
- Maroofian, Reza;
- Crosby, Andrew
Publication type:
Article
Erratum to: Epigenetic and genetic variation in GATA5 is associated with gastric disease risk.
Published in:
2016
By:
- Sobota, Rafal;
- Kodaman, Nuri;
- Mera, Robertino;
- Piazuelo, M.;
- Bravo, Luis;
- Pazos, Alvaro;
- Zabaleta, Jovanny;
- Delgado, Alberto;
- El-Rifai, Wael;
- Morgan, Douglas;
- Wilson, Keith;
- Correa, Pelayo;
- Williams, Scott;
- Schneider, Barbara
Publication type:
Erratum
The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature.
Published in:
Human Genetics, 2016, v. 135, n. 8, p. 841, doi. 10.1007/s00439-016-1675-5
By:
- Sinajon, Pierre;
- Verbaan, Deborah;
- So, Joyce
Publication type:
Article