Zoekresultaten - Jamshidi, Yalda

The genetics of pro-arrhythmic adverse drug reactions door Petropoulou, Evmorfia, Jamshidi, Yalda, Behr, Elijah R

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Causal graphs for the analysis of genetic cohort data door Hines, Oliver, Diaz-Ordaz, Karla, Vansteelandt, Stijn, Jamshidi, Yalda

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Novel genes for QTc interval. How much heritability is explained, and how much is left to find? door Jamshidi, Yalda, Nolte, Ilja M, Spector, Timothy D, Snieder, Harold

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Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma door Park, Soo, Jamshidi, Yalda, Vaideanu, Daniela, Fraser, Scott, Sowden, Jane C.

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The SH2B gene is associated with serum leptin and body fat in normal female twins door Jamshidi, Yalda, Snieder, Harold, Ge, Dongliang, Spector, Tim D, O’Dell, Sandra D

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Common polymorphisms in the SOCS3 gene are not associated with body weight, insulin sensitivity or lipid profile in normal female twins door Jamshidi, Yalda, Snieder, Harold, Wang, Xiaoling, Spector, Tim D, Carter, Nicholas D, O’Dell, Sandra D

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Testicular expression of TDRD1, TDRD5, TDRD9 and TDRD12 in azoospermia door Babakhanzadeh, Emad, Khodadadian, Ali, Rostami, Saadi, Alipourfard, Iraj, Aghaei, Mohsen, Nazari, Majid, Hosseinnia, Mehdi, Mehrjardi, Mohammad Yahya Vahidi, Jamshidi, Yalda, Ghasemi, Nasrin

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MicroRNA-153 targeting of KCNQ4 contributes to vascular dysfunction in hypertension door Carr, Georgina, Barrese, Vincenzo, Stott, Jennifer B., Povstyan, Oleksandr V., Jepps, Thomas A., Figueiredo, Hericka B., Zheng, Dongling, Jamshidi, Yalda, Greenwood, Iain A.

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Common STAT3 variants are not associated with obesity or insulin resistance in female twins door Jamshidi, Yalda, Kyriakou, Theodosios, Gooljar, Sakina B, Collins, Laura J, Lane, Carl A, Snieder, Harold, Wang, Xiaoling, Spector, Tim D, O'Dell, Sandra D

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Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy door Cauley, Edmund S., Pittman, Alan, Mummidivarpu, Swati, Karimiani, Ehsan G., Martinez, Samantha, Moroni, Isabella, Boostani, Reza, Podini, Daniele, Mora, Marina, Jamshidi, Yalda, Hoffman, Eric P., Manzini, M. Chiara

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Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardi... door Jones, Edward G., Mazaheri, Neda, Maroofian, Reza, Zamani, Mina, Seifi, Tahereh, Sedaghat, Alireza, Shariati, Gholamreza, Jamshidi, Yalda, Allen, Hugh D., Wehrens, Xander H. T., Galehdari, Hamid, Landstrom, Andrew P.

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Multiple roles of integrin-α3 at the neuromuscular junction door Ross, Jacob A., Webster, Richard G., Lechertier, Tanguy, Reynolds, Louise E., Turmaine, Mark, Bencze, Maximilien, Jamshidi, Yalda, Cetin, Hakan, Muntoni, Francesco, Beeson, David, Hodilvala-Dilke, Kairbaan, Conti, Francesco J.

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Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice door Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio

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The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice door Forzano, Francesca, Antonova, Olga, Clarke, Angus, de Wert, Guido, Hentze, Sabine, Jamshidi, Yalda, Moreau, Yves, Perola, Markus, Prokopenko, Inga, Read, Andrew, Reymond, Alexandre, Stefansdottir, Vigdis, van El, Carla, Genuardi, Maurizio

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Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3 door Osborn, Daniel Peter Sayer, Emrahi, Leila, Clayton, Joshua, Tabrizi, Mehrnoush Toufan, Wan, Alex Yui Bong, Maroofian, Reza, Yazdchi, Mohammad, Garcia, Michael Leon Enrique, Galehdari, Hamid, Hesse, Camila, Shariati, Gholamreza, Mazaheri, Neda, Sedaghat, Alireza, Goullée, Hayley, Laing, Nigel, Jamshidi, Yalda, Tajsharghi, Homa

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B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycan... door Maroofian, Reza, Riemersma, Moniek, Jae, Lucas T., Zhianabed, Narges, Willemsen, Marjolein H., Wissink-Lindhout, Willemijn M., Willemsen, Michèl A., de Brouwer, Arjan P. M., Mehrjardi, Mohammad Yahya Vahidi, Ashrafi, Mahmoud Reza, Kusters, Benno, Kleefstra, Tjitske, Jamshidi, Yalda, Nasseri, Mojila, Pfundt, Rolph, Brummelkamp, Thijn R., Abbaszadegan, Mohammad Reza, Lefeber, Dirk J., van Bokhoven, Hans

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Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24 door Hedberg-Oldfors, Carola, Abramsson, Alexandra, Osborn, Daniel P S, Danielsson, Olof, Fazlinezhad, Afsoon, Nilipour, Yalda, Hübbert, Laila, Nennesmo, Inger, Visuttijai, Kittichate, Bharj, Jaipreet, Petropoulou, Evmorfia, Shoreim, Azza, Vona, Barbara, Ahangari, Najmeh, López, Marcela Dávila, Doosti, Mohammad, Banote, Rakesh Kumar, Maroofian, Reza, Edling, Malin, Taherpour, Mehdi, Zetterberg, Henrik, Karimiani, Ehsan Ghayoor, Oldfors, Anders, Jamshidi, Yalda

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Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking door Wang, Haicui, Kaçar Bayram, Ayşe, Sprute, Rosanne, Ozdemir, Ozkan, Cooper, Emily, Pergande, Matthias, Efthymiou, Stephanie, Nedic, Ivana, Mazaheri, Neda, Stumpfe, Katharina, Azizi Malamiri, Reza, Shariati, Gholamreza, Zeighami, Jawaher, Bayram, Nurettin, Naghibzadeh, Seyed Kianoosh, Tajik, Mohamad, Yaşar, Mehmet, Sami Güven, Ahmet, Bibi, Farah, Sultan, Tipu, Salpietro, Vincenzo, Houlden, Henry, Per, Hüseyin, Galehdari, Hamid, Shalbafan, Bita, Jamshidi, Yalda, Cirak, Sebahattin

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Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy door Osborn, Daniel P.S., Pond, Heather L., Mazaheri, Neda, Dejardin, Jeremy, Munn, Christopher J., Mushref, Khaloob, Cauley, Edmund S., Moroni, Isabella, Pasanisi, Maria Barbara, Sellars, Elizabeth A., Hill, R. Sean, Partlow, Jennifer N., Willaert, Rebecca K., Bharj, Jaipreet, Malamiri, Reza Azizi, Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza, Mora, Marina, Swan, Laura E., Voit, Thomas, Conti, Francesco J., Jamshidi, Yalda, Manzini, M. Chiara

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Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay door Lee, Sangmoon, Chen, Dillon Y., Zaki, Maha S., Maroofian, Reza, Houlden, Henry, Di Donato, Nataliya, Abdin, Dalia, Morsy, Heba, Mirzaa, Ghayda M., Dobyns, William B., McEvoy-Venneri, Jennifer, Stanley, Valentina, James, Kiely N., Mancini, Grazia M.S., Schot, Rachel, Kalayci, Tugba, Altunoglu, Umut, Karimiani, Ehsan Ghayoor, Brick, Lauren, Kozenko, Mariya, Jamshidi, Yalda, Manzini, M. Chiara, Beiraghi Toosi, Mehran, Gleeson, Joseph G.

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