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Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3394
By:
- Ganesh, Santhi K.;
- Tragante, Vinicius;
- Guo, Wei;
- Guo, Yiran;
- Lanktree, Matthew B.;
- Smith, Erin N.;
- Johnson, Toby;
- Castillo, Berta Almoguera;
- Barnard, John;
- Baumert, Jens;
- Chang, Yen-Pei Christy;
- Elbers, Clara C.;
- Farrall, Martin;
- Fischer, Mary E.;
- Franceschini, Nora;
- Gaunt, Tom R.;
- Gho, Johannes M.I.H.;
- Gieger, Christian;
- Gong, Yan;
- Isaacs, Aaron
Publication type:
Article
Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3363, doi. 10.1093/hmg/ddt185
By:
- Sulkava, Sonja;
- Ollila, Hanna M.;
- Ahola, Kirsi;
- Partonen, Timo;
- Viitasalo, Katriina;
- Kettunen, Johannes;
- Lappalainen, Maarit;
- Kivimäki, Mika;
- Vahtera, Jussi;
- Lindström, Jaana;
- Härmä, Mikko;
- Puttonen, Sampsa;
- Salomaa, Veikko;
- Paunio, Tiina
Publication type:
Article
Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3227, doi. 10.1093/hmg/ddt176
By:
- Lee, Jong-Min;
- Galkina, Ekaterina I.;
- Levantovsky, Rachel M.;
- Fossale, Elisa;
- Anne Anderson, Mary;
- Gillis, Tammy;
- Srinidhi Mysore, Jayalakshmi;
- Coser, Kathryn R.;
- Shioda, Toshi;
- Zhang, Bin;
- Furia, Matthew D.;
- Derry, Jonathan;
- Kohane, Isaac S.;
- Seong, Ihn Sik;
- Wheeler, Vanessa C.;
- Gusella, James F.;
- MacDonald, Marcy E.
Publication type:
Article
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3381, doi. 10.1093/hmg/ddt189
By:
- Reiner, Alexander P.;
- Hartiala, Jaana;
- Zeller, Tanja;
- Bis, Joshua C.;
- Dupuis, Josée;
- Fornage, Myriam;
- Baumert, Jens;
- Kleber, Marcus E.;
- Wild, Philipp S.;
- Baldus, Stephan;
- Bielinski, Suzette J.;
- Fontes, João D.;
- Illig, Thomas;
- Keating, Brendan J.;
- Lange, Leslie A.;
- Ojeda, Francisco;
- Müller-Nurasyid, Martina;
- Munzel, Thomas F.;
- Psaty, Bruce M.;
- Rice, Kenneth
Publication type:
Article
Editorial Board.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. NP, doi. 10.1093/hmg/ddt362
Publication type:
Article
Glucocorticoid receptor is required for foetal heart maturation.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3269, doi. 10.1093/hmg/ddt182
By:
- Rog-Zielinska, Eva A.;
- Thomson, Adrian;
- Kenyon, Christopher J.;
- Brownstein, David G.;
- Moran, Carmel M.;
- Szumska, Dorota;
- Michailidou, Zoi;
- Richardson, Jennifer;
- Owen, Elizabeth;
- Watt, Alistair;
- Morrison, Harris;
- Forrester, Lesley M.;
- Bhattacharya, Shoumo;
- Holmes, Megan C.;
- Chapman, Karen E.
Publication type:
Article
Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3195, doi. 10.1093/hmg/ddt173
By:
- Li, Hong;
- Sheridan, Ryan;
- Williams, Trevor
Publication type:
Article
Cover Page.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. NP, doi. 10.1093/hmg/ddt361
Publication type:
Article
Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3259, doi. 10.1093/hmg/ddt180
By:
- Korvatska, Olena;
- Strand, Nicholas S.;
- Berndt, Jason D.;
- Strovas, Tim;
- Chen, Dong-Hui;
- Leverenz, James B.;
- Kiianitsa, Konstantin;
- Mata, Ignacio F.;
- Karakoc, Emre;
- Greenup, J. Lynne;
- Bonkowski, Emily;
- Chuang, Joseph;
- Moon, Randall T.;
- Eichler, Evan E.;
- Nickerson, Deborah A.;
- Zabetian, Cyrus P.;
- Kraemer, Brian C.;
- Bird, Thomas D.;
- Raskind, Wendy H.
Publication type:
Article
The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3218, doi. 10.1093/hmg/ddt175
By:
- Abplanalp, Jeannette;
- Laczko, Endre;
- Philp, Nancy J.;
- Neidhardt, John;
- Zuercher, Jurian;
- Braun, Philipp;
- Schorderet, Daniel F.;
- Munier, Francis L.;
- Verrey, François;
- Berger, Wolfgang;
- Camargo, Simone M.R.;
- Kloeckener-Gruissem, Barbara
Publication type:
Article
Cytoglobin has bimodal: tumour suppressor and oncogene functions in lung cancer cell lines.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3207, doi. 10.1093/hmg/ddt174
By:
- Oleksiewicz, Urszula;
- Liloglou, Triantafillos;
- Tasopoulou, Kalliopi-Maria;
- Daskoulidou, Nikoleta;
- Bryan, Julie;
- Gosney, John R.;
- Field, John K.;
- Xinarianos, George
Publication type:
Article
Genome-wide association study of age at menarche in African-American women.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3329, doi. 10.1093/hmg/ddt181
By:
- Demerath, Ellen W.;
- Liu, Ching-Ti;
- Franceschini, Nora;
- Chen, Gary;
- Palmer, Julie R.;
- Smith, Erin N.;
- Chen, Christina T.L.;
- Ambrosone, Christine B.;
- Arnold, Alice M.;
- Bandera, Elisa V.;
- Berenson, Gerald S.;
- Bernstein, Leslie;
- Britton, Angela;
- Cappola, Anne R.;
- Carlson, Christopher S.;
- Chanock, Stephen J.;
- Chen, Wei;
- Chen, Zhao;
- Deming, Sandra L.;
- Elks, Cathy E.
Publication type:
Article
Nilotinib reverses loss of dopamine neurons and improves motor behavior via autophagic degradation of α-synuclein in Parkinson's disease models.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3315, doi. 10.1093/hmg/ddt192
By:
- Hebron, Michaeline L.;
- Lonskaya, Irina;
- Moussa, Charbel E.-H.
Publication type:
Article
Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3306, doi. 10.1093/hmg/ddt187
By:
- Van Maldergem, Lionel;
- Hou, Qingming;
- Kalscheuer, Vera M.;
- Rio, Marlène;
- Doco-Fenzy, Martine;
- Medeira, Ana;
- de Brouwer, Arjan P.M.;
- Cabrol, Christelle;
- Haas, Stefan A.;
- Cacciagli, Pierre;
- Moutton, Sébastien;
- Landais, Emilie;
- Motte, Jacques;
- Colleaux, Laurence;
- Bonnet, Céline;
- Villard, Laurent;
- Dupont, Juliette;
- Man, Heng-Ye
Publication type:
Article
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3347
By:
- Zhao, Shuang-Xia;
- Xue, Li-Qiong;
- Liu, Wei;
- Gu, Zhao-Hui;
- Pan, Chun-Ming;
- Yang, Shao-Ying;
- Zhan, Ming;
- Wang, Hai-Ning;
- Liang, Jun;
- Gao, Guan-Qi;
- Zhang, Xiao-Mei;
- Yuan, Guo-Yue;
- Li, Chang-Gui;
- Du, Wen-Hua;
- Liu, Bing-Li;
- Liu, Li-Bin;
- Chen, Gang;
- Su, Qing;
- Peng, Yong-De;
- Zhao, Jia-Jun
Publication type:
Article
Investigation of six testicular germ cell tumor susceptibility genes suggests a parent-of-origin effect in SPRY4.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3373, doi. 10.1093/hmg/ddt188
By:
- Karlsson, Robert;
- Andreassen, Kristine E.;
- Kristiansen, Wenche;
- Aschim, Elin L.;
- Bremnes, Roy M.;
- Dahl, Olav;
- Fosså, Sophie D.;
- Klepp, Olbjørn;
- Langberg, Carl W.;
- Solberg, Arne;
- Tretli, Steinar;
- Magnusson, Patrik K.E.;
- Adami, Hans-Olov;
- Haugen, Trine B.;
- Grotmol, Tom;
- Wiklund, Fredrik
Publication type:
Article
Contents Page.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. NP, doi. 10.1093/hmg/ddt360
Publication type:
Article
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3187, doi. 10.1093/hmg/ddt171
By:
- Caputo, Valentina S.;
- Costa, Joana R.;
- Makarona, Kalliopi;
- Georgiou, Elisabeth;
- Layton, D. Mark;
- Roberts, Irene;
- Karadimitris, Anastasios
Publication type:
Article
ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3250, doi. 10.1093/hmg/ddt179
By:
- Yahyavi, Mani;
- Abouzeid, Hana;
- Gawdat, Ghada;
- de Preux, Anne-Sophie;
- Xiao, Tong;
- Bardakjian, Tanya;
- Schneider, Adele;
- Choi, Alex;
- Jorgenson, Eric;
- Baier, Herwig;
- El Sada, Mohamad;
- Schorderet, Daniel F.;
- Slavotinek, Anne M.
Publication type:
Article
Subscription Page.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. NP, doi. 10.1093/hmg/ddt363
Publication type:
Article
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3239, doi. 10.1093/hmg/ddt178
By:
- Le Guen, Tangui;
- Jullien, Laurent;
- Touzot, Fabien;
- Schertzer, Michael;
- Gaillard, Laetitia;
- Perderiset, Mylène;
- Carpentier, Wassila;
- Nitschke, Patrick;
- Picard, Capucine;
- Couillault, Gérard;
- Soulier, Jean;
- Fischer, Alain;
- Callebaut, Isabelle;
- Jabado, Nada;
- Londono-Vallejo, Arturo;
- de Villartay, Jean-Pierre;
- Revy, Patrick
Publication type:
Article
A high-content, high-throughput siRNA screen identifies cyclin D2 as a potent regulator of muscle progenitor cell fusion and a target to enhance muscle regeneration.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3283, doi. 10.1093/hmg/ddt184
By:
- Khanjyan, Michael V.;
- Yang, Jonathan;
- Kayali, Refik;
- Caldwell, Thomas;
- Bertoni, Carmen
Publication type:
Article
Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3296
By:
- López-Erauskin, J.;
- Galino, J.;
- Ruiz, M.;
- Cuezva, J.M.;
- Fabregat, I.;
- Cacabelos, D.;
- Boada, J.;
- Martínez, J.;
- Ferrer, I.;
- Pamplona, R.;
- Villarroya, F.;
- Portero-Otín, M.;
- Fourcade, S.;
- Pujol, A.
Publication type:
Article

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