Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: YY1AP1[original query] |
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The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. Genetics in medicine : official journal of the American College of Medical Genetics 2019 9 22 (2): 427-431. Pinard Amélie, Guey Stéphanie, Guo Dongchuan, Cecchi Alana C, Kharas Natasha, Wallace Stephanie, Regalado Ellen S, Hostetler Ellen M, Sharrief Anjail Z, Bergametti Françoise, Kossorotoff Manoelle, Hervé Dominique, Kraemer Markus, Bamshad Michael J, Nickerson Deborah A, Smith Edward R, Tournier-Lasserve Elisabeth, Milewicz Dianna |
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing. Circulation. Genomic and precision medicine 2020 10 13 (6): e003030. Carss Keren J, Baranowska Anna A, Armisen Javier, Webb Tom R, Hamby Stephen E, Premawardhana Diluka, Al-Hussaini Abtehale, Wood Alice, Wang Quanli, Deevi Sri V V, Vitsios Dimitrios, Lewis Samuel H, Kotecha Deevia, Bouatia-Naji Nabila, Hesselson Stephanie, Iismaa Siiri E, Tarr Ingrid, McGrath-Cadell Lucy, Muller David W, Dunwoodie Sally L, Fatkin Diane, Graham Robert M, Giannoulatou Eleni, Samani Nilesh J, Petrovski Slavé, Haefliger Carolina, Adlam Dav |
Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age. Nature communications 2022 Jul 13 (1): 3881. Burkhardt Birgit, Michgehl Ulf, Rohde Jonas, Erdmann Tabea, Berning Philipp, Reutter Katrin, Rohde Marius, Borkhardt Arndt, Burmeister Thomas, Dave Sandeep, Tzankov Alexandar, Dugas Martin, Sandmann Sarah, Fend Falko, Finger Jasmin, Mueller Stephanie, Gökbuget Nicola, Haferlach Torsten, Kern Wolfgang, Hartmann Wolfgang, Klapper Wolfram, Oschlies Ilske, Richter Julia, Kontny Udo, Lutz Mathias, Maecker-Kolhoff Britta, Ott German, Rosenwald Andreas, Siebert Reiner, von Stackelberg Arend, Strahm Brigitte, Woessmann Wilhelm, Zimmermann Martin, Zapukhlyak Myroslav, Grau Michael, Lenz Geo |
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