HuGE Literature Finder
Records
1
-
12
Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PloS one 2022 17 (8): e0273280. Przyby?a Weronika, Gjersvoll Paulsen Kirsti Marie, Mishra Charitra Kumar, Nygård Ståle, Engebretsen Solveig, Ruud Ellen, Trøen Gunhild, Beiske Klaus, Baumbusch Lars Oliv |
Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease. Molecular psychiatry 2022 3 27 (5): 2554-2562. Shigemizu Daichi, Asanomi Yuya, Akiyama Shintaro, Mitsumori Risa, Niida Shumpei, Ozaki Kouic |
Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy. Orphanet journal of rare diseases 2021 4 16 (1): 188. Zhang Shu, Qin Dongdong, Wu Liwen, Li Man, Song Lifang, Wei Cuijie, Lu Chunling, Zhang Xiaoli, Hong Siqi, Ma Mingming, Wu Shiwen, |
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy. European journal of heart failure 2021 5 23 (8): 1276-1286. Restrepo-Cordoba Maria A, Wahbi Karim, Florian Anca R, Jiménez-Jáimez Juan, Politano Luisa, Arad Michael, Climent-Paya Vicente, Garcia-Alvarez Ana, Hansen Rasmus B, Larrañaga-Moreira José M, Kubanek Milos, Lopes Luis R, Ros Andrea, Jurcut Ruxandra, Rasmussen Torsten B, Ruiz-Guerrero Luis, Pribe-Wolferts Regina, Palomino-Doza Julian, Bilinska Zofia, Rodríguez-Palomares José F, Van Loon Rosa L E, Basurte Elorz María Teresa, Quarta Giovanni, Robledo Iñarritu Maria, Verdonschot Job A J, Stojkovic Tanya, Shomanova Zornitsa, Bermudez-Jimenez Francisco, Palladino Alberto, Freimark Dov, García-Álvarez Maria I, Jorda Paloma, Dominguez Fernando, Ochoa Juan Pablo, Girolami Francesca, Brugada Ramon, Meder Benjamin, Barriales-Villa Roberto, Mogensen Jens, Laforêt Pascal, Yilmaz Ali, Elliott Perry, Garcia-Pavia Pablo, |
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome. Heart rhythm O2 2021 10 2 (5): 431-438. Giudicessi John R, Maleszewski Joseph J, Tester David J, Ackerman Michael |
The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy. Journal of cardiac failure 2020 Aug . Nagai Masashi, Awano Hiroyuki, Yamamoto Tetsushi, Bo Ryosuke, Matsuo Masafumi, Iijima Kazumo |
Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation. Journal of clinical medicine 2020 Jan 9 (2): . Vad Oliver Bundgaard, Paludan-Müller Christian, Ahlberg Gustav, Kalstø Silje Madeleine, Ghouse Jonas, Andreasen Laura, Haunsø Stig, Tveit Arnljot, Sajadieh Ahmad, Christophersen Ingrid Elisabeth, Svendsen Jesper Hastrup, Olesen Morten Salli |
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India. Neurology India 2018 1 66 (1): 77-82. Singh Ravinder-Jeet, Manjunath Mahadevappa, Preethish-Kumar Veeramani, Polavarapu Kiran, Vengalil Seena, Thomas Priya T, Thennarasu Kandavel, Gayathri Narayanappa, Sekar Deepha, Nashi Saraswati, Nalini Atchayar |
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy. PloS one 2015 10 (10): e0141240. Barp Andrea, Bello Luca, Politano Luisa, Melacini Paola, Calore Chiara, Polo Angela, Vianello Sara, Sorarù Gianni, Semplicini Claudio, Pantic Boris, Taglia Antonella, Picillo Ester, Magri Francesca, Gorni Ksenija, Messina Sonia, Vita Gian Luca, Vita Giuseppe, Comi Giacomo P, Ermani Mario, Calvo Vincenzo, Angelini Corrado, Hoffman Eric P, Pegoraro Ele |
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. European journal of heart failure 2013 Jan . van Spaendonck-Zwarts KY, van Rijsingen IA, van den Berg MP, Lekanne Deprez RH, Post JG, van Mil AM, Asselbergs FW, Christiaans I, van Langen IM, Wilde AA, de Boer RA, Jongbloed JD, Pinto YM, van Tintelen JP |
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy. Circulation 2005 Nov 112 (18): 2799-804. Jefferies John L, Eidem Benjamin W, Belmont John W, Craigen William J, Ware Stephanie M, Fernbach Susan D, Neish Steven R, Smith E O'brian, Towbin Jeffrey |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 28, 2023
- Content source: