Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: MFAP4[original query] |
---|
Search on chromosome 17 centromere reveals TNFRSF13B as a susceptibility gene for intracranial aneurysm: a preliminary study. Circulation 2006 Apr 113 (16): 2002-10. Inoue Kayoko, Mineharu Youhei, Inoue Sumiko, Yamada Shigeki, Matsuda Fumihiko, Nozaki Kazuhiko, Takenaka Katsunobu, Hashimoto Nobuo, Koizumi Ak |
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clinical genetics 2007 Jun 71 (6): 540-50. Edelman E A, Girirajan S, Finucane B, Patel P I, Lupski J R, Smith A C M, Elsea S |
Rare copy number variants contribute to congenital left-sided heart disease. PLoS genetics 2012 Sep 8 (9): e1002903. Hitz Marc-Phillip, Lemieux-Perreault Louis-Philippe, Marshall Christian, Feroz-Zada Yassamin, Davies Robbie, Yang Shi Wei, Lionel Anath Christopher, D'Amours Guylaine, Lemyre Emmanuelle, Cullum Rebecca, Bigras Jean-Luc, Thibeault Maryse, Chetaille Philippe, Montpetit Alexandre, Khairy Paul, Overduin Bert, Klaassen Sabine, Hoodless Pamela, Awadalla Philip, Hussin Julie, Idaghdour Youssef, Nemer Mona, Stewart Alexandre F R, Boerkoel Cornelius, Scherer Stephen W, Richter Andrea, Dubé Marie-Pierre, Andelfinger Greg |
Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development. Nature communications 2024 1 15 (1): 528. Amil M Shah, Peder L Myhre, Victoria Arthur, Pranav Dorbala, Humaira Rasheed, Leo F Buckley, Brian Claggett, Guning Liu, Jianzhong Ma, Ngoc Quynh Nguyen, Kunihiro Matsushita, Chiadi Ndumele, Adrienne Tin, Kristian Hveem, Christian Jonasson, Håvard Dalen, Eric Boerwinkle, Ron C Hoogeveen, Christie Ballantyne, Josef Coresh, Torbjørn Omland, Bing |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: