Deep sequencing reveals 50 novel genes for recessive cognitive disorders
NAJMABADI, Hossein, HAO HU, ZECHA, Agnes, MOHSENI, Marzieh, PUTTMANN, Lucia, LEYLA NOURI VAHID, JENSEN, Corinna, LIA ABBASI MOHEB, BIENEK, Melanie, LARTI, Farzaneh, MUELLER, Ines, WEISSMANN, Robert, GARSHASBI, Masoud, DARVISH, Hossein, WROGEMANN, Klaus, HADAVI, Valeh, LIPKOWITZ, Bettina, ESMAEELI-NIEH, Sahar, WIECZOREK, Dagmar, KARIMINEJAD, Roxana, SAGHAR GHASEMI FIROUZABADI, COHEN, Monika, FATTAHI, Zohreh, ZEMOJTEL, Tomasz, ROST, Imma, MOJAHEDI, Faezeh, HERTZBERG, Christoph, DEHGHAN, Atefeh, RAJAB, Anna, MOHAMMAD JAVAD SOLTANI BANAVANDI, HOFFER, Julia, FALAH, Masoumeh, MUSANTE, Luciana, KALSCHEUER, Vera, SEYEDEH SEDIGHEH ABEDINI, ULLMANN, Reinhard, WALTER KUSS, Andreas, TZSCHACH, Andreas, KAHRIZI, Kimia, ROPERS, H. Hilger, WEI CHEN, HOSSEINI, Masoumeh, BEHJATI, Farkhondeh, HAAS, Stefan, JAMALI, Payman
Published in Nature (London) (06.10.2011)
Published in Nature (London) (06.10.2011)
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Journal Article
Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease
Seyedtaghia, Mohammad Reza, Soudyab, Mohammad, Shariati, Mohammad, Esfehani, Reza Jafarzadeh, Vafadar, Shabnam, Shalaei, Neda, Nouri, Vahid, Zech, Michael, Winkelmann, Julianne, shoeibi, Ali, Sadr-Nabavi, Ariane
Published in Heliyon (01.04.2023)
Published in Heliyon (01.04.2023)
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Journal Article
A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family
Garshasbi, Masoud, Kahrizi, Kimia, Hosseini, Masoumeh, Nouri Vahid, Leila, Falah, Masoumeh, Hemmati, Sahel, Hu, Hao, Tzschach, Andreas, Ropers, Hans Hilger, Najmabadi, Hossein, Kuss, Andreas Walter
Published in American journal of medical genetics. Part A (01.08.2011)
Published in American journal of medical genetics. Part A (01.08.2011)
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Journal Article
COVID-19 pandemic and health worker stress: The mediating effect of emotional regulation
García-Batista, Zoilo Emilio, Guerra-Peña, Kiero, Nouri Kandany, Vahid, Marte, María Isabel, Garrido, Luis Eduardo, Cantisano-Guzmán, Luisa Marilia, Moretti, Luciana, Medrano, Leonardo Adrián
Published in PloS one (24.11.2021)
Published in PloS one (24.11.2021)
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Journal Article
Genetics of intellectual disability in consanguineous families
Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Herwig, Ralf, Hosseini, Masoumeh, Oppitz, Cornelia, Abedini, Seyedeh Sedigheh, Suckow, Vanessa, Larti, Farzaneh, Beheshtian, Maryam, Lipkowitz, Bettina, Akhtarkhavari, Tara, Mehvari, Sepideh, Otto, Sabine, Mohseni, Marzieh, Arzhangi, Sanaz, Jamali, Payman, Mojahedi, Faezeh, Taghdiri, Maryam, Papari, Elaheh, Soltani Banavandi, Mohammad Javad, Akbari, Saeide, Tonekaboni, Seyed Hassan, Dehghani, Hossein, Ebrahimpour, Mohammad Reza, Bader, Ingrid, Davarnia, Behzad, Cohen, Monika, Khodaei, Hossein, Albrecht, Beate, Azimi, Sarah, Zirn, Birgit, Bastami, Milad, Wieczorek, Dagmar, Bahrami, Gholamreza, Keleman, Krystyna, Vahid, Leila Nouri, Tzschach, Andreas, Gärtner, Jutta, Gillessen-Kaesbach, Gabriele, Varaghchi, Jamileh Rezazadeh, Timmermann, Bernd, Pourfatemi, Fatemeh, Jankhah, Aria, Chen, Wei, Nikuei, Pooneh, Kalscheuer, Vera M, Oladnabi, Morteza, Wienker, Thomas F, Ropers, Hans-Hilger, Najmabadi, Hossein
Published in Molecular psychiatry (01.07.2019)
Published in Molecular psychiatry (01.07.2019)
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Journal Article
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
Abbasi-Moheb, Lia, Mertel, Sara, Gonsior, Melanie, Nouri-Vahid, Leyla, Kahrizi, Kimia, Cirak, Sebahattin, Wieczorek, Dagmar, Motazacker, M. Mahdi, Esmaeeli-Nieh, Sahar, Cremer, Kirsten, Weißmann, Robert, Tzschach, Andreas, Garshasbi, Masoud, Abedini, Seyedeh S., Najmabadi, Hossein, Ropers, H. Hilger, Sigrist, Stephan J., Kuss, Andreas W.
Published in American journal of human genetics (04.05.2012)
Published in American journal of human genetics (04.05.2012)
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Journal Article
Whole-Exome Sequencing Study of Consanguineous Parkinson’s Disease Families and Related Phenotypes: Report of Twelve Novel Variants
Soudyab, Mohammad, Shariati, Mohammad, Esfehani, Reza Jafarzadeh, Shalaei, Neda, Vafadar, Shabnam, Nouri, Vahid, Zech, Michael, Winkelmann, Julianne, Shoeibi, Ali, Sadr-Nabavi, Ariane
Published in Journal of molecular neuroscience (01.12.2022)
Published in Journal of molecular neuroscience (01.12.2022)
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Journal Article
El desempeño del ChatGPT en la resolución de un examen de residencia médica: ¿un indicador de la evolución de inteligencia artificial en educación médica?
Valdez, Pascual, Nouri Kandany, Vahid, Valdez Disla, Alexander
Published in Ciencia y Salud (Santo Domingo. En línea) (01.06.2024)
Published in Ciencia y Salud (Santo Domingo. En línea) (01.06.2024)
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Journal Article
Creencias, actitudes y prácticas del médico en rol de paciente: perspectivas en República Dominicana
Nouri Kandany, Vahid, Peña Núñez, Melani, Aponte Báez, Erick, Pimentel Brito, Darlin, Toribio González, Jaily, Gómez Muñoz, Heidy
Published in Ciencia y Salud (Santo Domingo. En línea) (03.06.2023)
Published in Ciencia y Salud (Santo Domingo. En línea) (03.06.2023)
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Journal Article
Comparación de los valores de Spo2 de los dedos de las manos en una población sana
Nouri Kandany, Vahid, Pena Núñez, Melani, Marte, María Isabel, Capellán Álvarez, Oliber, Pérez Peña, Ibrahim, De León Cruz, Esmayanson
Published in Ciencia y Salud (Santo Domingo. En línea) (19.11.2022)
Published in Ciencia y Salud (Santo Domingo. En línea) (19.11.2022)
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Journal Article
Creencias, actitudes y prácticas del médico en situacion de paciente: Encuesta en línea realizada en países latinoamericanos
Nouri, Vahid, Valdez, Pascual, Puello-Galarcio, Homero, Bisso, Aland, Palencia-Vizcarra, Rodolfo, Rodríguez-Hurtado, Diana
Published in Revista de la Sociedad Peruana de Medicina Interna (26.12.2022)
Published in Revista de la Sociedad Peruana de Medicina Interna (26.12.2022)
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Journal Article
Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease
Seyedtaghia, Mohammad Reza, Soudyab, Mohammad, Shariati, Mohammad, Esfehani, Reza Jafarzadeh, Vafadar, Shabnam, Shalaei, Neda, Nouri, Vahid, Zech, Michael, Winkelmann, Julianne, Shoeibi, Ali, Sadr-Nabavi, Ariane
Published in Heliyon (01.04.2023)
Published in Heliyon (01.04.2023)
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A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family
Garshasbi, Masoud, Kahrizi, Kimia, Hosseini, Masoumeh, Nouri Vahid, Leila, Falah, Masoumeh, Hemmati, Sahel, Hu, Hao, Tzschach, Andreas, Ropers, Hans Hilger, Najmabadi, Hossein, Kuss, Andreas Walter
Published in American Journal of Medical Genetics Part A (01.08.2011)
Published in American Journal of Medical Genetics Part A (01.08.2011)
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Comparación de los valores de spo2 de los dedosde las manos en una población sana
Marte, María Isabel, Capellán Álvarez, Oliber, de León Cruz, Esmayanson, Nouri Kandany, Vahid, Pena Núñez, Melani, Pérez Peña, Ibrahim
Published in Ciencia y Salud (Santo Domingo. En línea) (2022)
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Published in Ciencia y Salud (Santo Domingo. En línea) (2022)
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