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Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies Vaseghi, Parisa; Habibi, Laleh; Neidich, Julie A.; Cao, Yang; Fattahi, Neda; Rashidi-Nezhad, Ramin; Salehnezhad, Tayebeh; Dalili, Hossein; Sharbaf, Fatemeh Rahimi; Zarkesh, Mohammad Reza; Malekian, Mahtash; Mokhberdezfuli, Mahdieh; Mehrtash, Amirhosein; Ardeshirdavani, Amin; Kariminejad, Roxana; Ghorbansabagh, Vafa; Sadeghimoghadam, Parvane; Naddaf, Amir; Shirvany, Tahereh Esmaeilnia; Mosayebi, Ziba; Sahebdel, Behrokh; Golshahi, Fatemeh; Shirazi, Mahboobeh; Shamel, Shirin; Moeini, Roksana; Heidari, Abolfazl; Daneshmand, Mohammad Ali; Ghasemi, Reza; Akrami, Seyed Mohammad; Rashidi-Nezhad, Ali 分享 收藏
Recommendations for whole genome sequencing in diagnostics for rare diseases Souche, Erika; Beltran, Sergi; Brosens, Erwin; Belmont, John W.; Fossum, Magdalena; Riess, Olaf; Gilissen, Christian; Ardeshirdavani, Amin; Houge, Gunnar; van Gijn, Marielle; Clayton-Smith, Jill; Synofzik, Matthis; de Leeuw, Nicole; Deans, Zandra C.; Dincer, Yasemin; Eck, Sebastian H.; van eer Crabben, Saskia; Balasubramanian, Meena; Graessner, Holm; Sturm, Marc; Firth, Helen; Ferlini, Alessandra; Nabbout, Rima; De Baere, Elfride; Liehr, Thomas; Macek, Milan; Matthijs, Gert; Scheffer, Hans; Bauer, Peter; Yntema, Helger G.; Weiss, Marjan M. 分享 收藏
Associations of Disease-Modifying Therapies With COVID-19 Severity in Multiple Sclerosis 多发性硬化症中疾病修饰疗法与新型冠状病毒肺炎严重程度的关联 Simpson-Yap, Steve; De Brouwer, Edward; Kalincik, Tomas; Rijke, Nick; Hillert, Jan A.; Walton, Clare; Edan, Gilles; Moreau, Yves; Spelman, Tim; Geys, Lotte; Parciak, Tina; Gautrais, Clement; Lazovski, Nikola; Pirmani, Ashkan; Ardeshirdavanai, Amin; Forsberg, Lars; Glaser, Anna; McBurney, Robert; Schmidt, Hollie; Bergmann, Arnfin B.; Braune, Stefan; Stahmann, Alexander; Middleton, Rodden; Salter, Amber; Fox, Robert J.; van der Walt, Anneke; Butzkueven, Helmut; Alroughani, Raed; Ozakbas, Serkan; Rojas, Juan, I; van der Mei, Ingrid; Nag, Nupur; Ivanov, Rumen; do Olival, Guilherme Sciascia; Dias, Alice Estavo; Magyari, Melinda; Brum, Doralina; Mendes, Maria Fernanda; Alonso, Ricardo N.; Nicholas, Richard S.; Bauer, Johana; Chertcoff, Anibal Sebastian; Zabalza, Anna; Arrambide, Georgina; Fidao, Alexander; Comi, Giancarlo; Peeters, Liesbet 分享 收藏
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Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome Zemojtel, Tomasz; koehler, Sebastian; Mackenroth, Luisa; Jaeger, Marten; Hecht, Jochen; Krawitz, Peter; Graul-Neumann, Luitgard; Doelken, Sandra; Ehmke, Nadja; Spielmann, Malte; Oien, Nancy Christine; Schweiger, Michal R.; Krueger, Ulrike; Frommer, Goetz; Fischer, Bjoern; Kornak, Uwe; Floettmann, Ricarda; Ardeshirdavani, Amin; Moreau, Yves; Lewis, Suzanna E.; Haendel, Melissa; Smedley, Damian; Horn, Denise; Mundlos, Stefan; Robinson, Peter N. 分享 收藏
eXtasy: variant prioritization by genomic data fusion Sifrim, Alejandro; Popovic, Dusan; Tranchevent, Leon-Charles; Ardeshirdavani, Amin; Sakai, Ryo; Konings, Peter; Vermeesch, Joris R.; Aerts, Jan; De Moor, Bart; Moreau, Yves 分享 收藏
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