Works matching IS 15537390 AND DT 2018 AND VI 14 AND IP 5


Results: 54
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    Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007329
    By:
    • Rivas, Manuel A.;
    • Avila, Brandon E.;
    • Koskela, Jukka;
    • Huang, Hailiang;
    • Stevens, Christine;
    • Pirinen, Matti;
    • Haritunians, Talin;
    • Neale, Benjamin M.;
    • Kurki, Mitja;
    • Ganna, Andrea;
    • Graham, Daniel;
    • Glaser, Benjamin;
    • Peter, Inga;
    • Atzmon, Gil;
    • Barzilai, Nir;
    • Levine, Adam P.;
    • Schiff, Elena;
    • Pontikos, Nikolas;
    • Weisburd, Ben;
    • Lek, Monkol
    Publication type:
    Article
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    Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

    Published in:
    2018
    By:
    • Liang, Jingjing;
    • Le, Thu H.;
    • Velez Edwards, Digna R.;
    • Tayo, Bamidele O.;
    • Gaulton, Kyle J.;
    • Smith, Jennifer A.;
    • Lu, Yingchang;
    • Jensen, Richard A.;
    • Chen, Guanjie;
    • Yanek, Lisa R.;
    • Schwander, Karen;
    • Tajuddin, Salman M.;
    • Sofer, Tamar;
    • Kim, Wonji;
    • Kayima, James;
    • McKenzie, Colin A.;
    • Fox, Ervin;
    • Nalls, Michael A.;
    • Young, J. Hunter;
    • Sun, Yan V.
    Publication type:
    Correction Notice
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    A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007386
    By:
    • Gonçalves, Sara;
    • Patat, Julie;
    • Guida, Maria Clara;
    • Lachaussée, Noelle;
    • Arrondel, Christelle;
    • Helmstädter, Martin;
    • Boyer, Olivia;
    • Gribouval, Olivier;
    • Gubler, Marie-Claire;
    • Mollet, Geraldine;
    • Rio, Marlène;
    • Charbit, Marina;
    • Bole-Feysot, Christine;
    • Nitschke, Patrick;
    • Huber, Tobias B.;
    • Wheeler, Patricia G.;
    • Haynes, Devon;
    • Juusola, Jane;
    • Billette de Villemeur, Thierry;
    • Nava, Caroline
    Publication type:
    Article
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    Population-specific genetic modification of Huntington's disease in Venezuela.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007274
    By:
    • Chao, Michael J.;
    • Kim, Kyung-Hee;
    • Shin, Jun Wan;
    • Lucente, Diane;
    • Wheeler, Vanessa C.;
    • Li, Hong;
    • Roach, Jared C.;
    • Hood, Leroy;
    • Wexler, Nancy S.;
    • Jardim, Laura B.;
    • Holmans, Peter;
    • Jones, Lesley;
    • Orth, Michael;
    • Kwak, Seung;
    • MacDonald, Marcy E.;
    • Gusella, James F.;
    • Lee, Jong-Min
    Publication type:
    Article
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    Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.

    Published in:
    2018
    By:
    • Watson-Scales, Sheona;
    • Kalmar, Bernadett;
    • Lana-Elola, Eva;
    • Gibbins, Dorota;
    • La Russa, Federica;
    • Wiseman, Frances;
    • Williamson, Matthew;
    • Saccon, Rachele;
    • Slender, Amy;
    • Olerinyova, Anna;
    • Mahmood, Radma;
    • Nye, Emma;
    • Cater, Heather;
    • Wells, Sara;
    • Yu, Y. Eugene;
    • Bennett, David L. H.;
    • Greensmith, Linda;
    • Fisher, Elizabeth M. C.;
    • Tybulewicz, Victor L. J.
    Publication type:
    Abstract
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    The receptor protein tyrosine phosphatase CLR-1 is required for synaptic partner recognition.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007312
    By:
    • Varshney, Aruna;
    • Benedetti, Kelli;
    • Watters, Katherine;
    • Shankar, Raakhee;
    • Tatarakis, David;
    • Coto Villa, Doris;
    • Magallanes, Khristina;
    • Agenor, Venia;
    • Wung, William;
    • Farah, Fatima;
    • Ali, Nebat;
    • Le, Nghi;
    • Pyle, Jacqueline;
    • Farooqi, Amber;
    • Kieu, Zanett;
    • Bremer, Martina;
    • VanHoven, Miri
    Publication type:
    Article
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    De novo and inherited private variants in MAP1B in periventricular nodular heterotopia.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007281
    By:
    • Heinzen, Erin L.;
    • O'Neill, Adam C.;
    • Zhu, Xiaolin;
    • Allen, Andrew S.;
    • Bahlo, Melanie;
    • Chelly, Jamel;
    • Dobyns, William B.;
    • Freytag, Saskia;
    • Guerrini, Renzo;
    • Leventer, Richard J.;
    • Poduri, Annapurna;
    • Robertson, Stephen P.;
    • Walsh, Christopher A.;
    • Zhang, Mengqi;
    • null, null
    Publication type:
    Article
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