Deep sequencing reveals 50 novel genes for recessive cognitive disorders von Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman, Zecha, Agnes, Mohseni, Marzieh, Püttmann, Lucia, Vahid, Leyla Nouri, Jensen, Corinna, Moheb, Lia Abbasi, Bienek, Melanie, Larti, Farzaneh, Mueller, Ines, Weissmann, Robert, Darvish, Hossein, Wrogemann, Klaus, Hadavi, Valeh, Lipkowitz, Bettina, Esmaeeli-Nieh, Sahar, Wieczorek, Dagmar, Kariminejad, Roxana, Firouzabadi, Saghar Ghasemi, Cohen, Monika, Fattahi, Zohreh, Rost, Imma, Mojahedi, Faezeh, Hertzberg, Christoph, Dehghan, Atefeh, Rajab, Anna, Banavandi, Mohammad Javad Soltani, Hoffer, Julia, Falah, Masoumeh, Musante, Luciana, Kalscheuer, Vera, Ullmann, Reinhard, Kuss, Andreas Walter, Tzschach, Andreas, Kahrizi, Kimia, Ropers, H. Hilger

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COVID-19 pandemic and health worker stress: The mediating effect of emotional regulation von Emilio Garcia-Batista, Zoilo, Guerra-Pena, Kiero, Nouri Kandany, Vahid, Isabel Marte, Maria, Eduardo Garrido, Luis, Marilia Cantisano-Guzman, Luisa, Moretti, Luciana, Adrian Medrano, Leonardo

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A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family von 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

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Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease von 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

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Genetics of intellectual disability in consanguineous families von 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

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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability von 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.

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Integrating Type-1 Fuzzy and Type-2 Fuzzy Clustering with K-Means for Pre-Processing Input Data in Classification Algorithms von Nouri, Vahid

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Whole-Exome Sequencing Study of Consanguineous Parkinson’s Disease Families and Related Phenotypes: Report of Twelve Novel Variants von Soudyab, Mohammad, Shariati, Mohammad, Esfehani, Reza Jafarzadeh, Shalaei, Neda, Vafadar, Shabnam, Nouri, Vahid, Zech, Michael, Winkelmann, Julianne, Shoeibi, Ali, Sadr-Nabavi, Ariane

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Percepción de la población sobre la vacuna contra el COVID-19: perspectivas en República Dominicana, 2020 von Nouri Kandanya, Vahid, Marte, María Isabel, Pichardo, Elly

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Creencias, actitudes y prácticas del médico en situacion de paciente: Encuesta en línea realizada en países latinoamericanos von Nouri, Vahid, Valdez, Pascual, Puello-Galarcio, Homero, Bisso, Aland, Palencia-Vizcarra, Rodolfo, Rodríguez-Hurtado, Diana

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USE OF A RELEASE CONTROL AGENT IN A NICOTINE COMPOSITION von ABRAHAMIAN, Ara, NOURI, Vahid

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NICOTINE COMPOSITION von ABRAHAMIAN, Ara, NOURI, Vahid

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Análisis de la percepción del programa de formación de médicos residentes de medicina interna en Latinoamérica: una encuesta de opinión von Nouri Kandany, Vahid, Valdez, Pascual, Bisso, Aland, Puello-Galarcio, Homero, Palencia-Vizcarra, Rodolfo, Rodríguez-Hurtado, Diana

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NICOTINE COMPOSITION von ABRAHAMIAN, Ara, NOURI, Vahid

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Creencias, actitudes y prácticas del médico en rol de paciente: perspectivas en República Dominicana von Nouri Kandany, Vahid, Peña Núñez, Melani, Aponte Báez, Erick, Pimentel Brito, Darlin, Toribio González, Jaily, Gómez Muñoz, Heidy

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Comparación de los valores de Spo2 de los dedos de las manos en una población sana von Nouri Kandany, Vahid, Pena Núñez, Melani, Marte, María Isabel, Capellán Álvarez, Oliber, Pérez Peña, Ibrahim, De León Cruz, Esmayanson

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El desempeño del ChatGPT en la resolución de un examen de residencia médica: ¿un indicador de la evolución de inteligencia artificial en educación médica? von Alexander Valdez Disla, Vahid Nouri Kandany, Pascual Valdez

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Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease von Seyedtaghia, Mohammad Reza, Soudyab, Mohammad, Shariati, Mohammad, Esfehani, Reza Jafarzadeh, Vafadar, Shabnam, Shalaei, Neda, Nouri, Vahid, Zech, Michael, Winkelmann, Juliane, Shoeibi, Ali, Sadr-Nabavi, Ariane

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Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease von 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

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El desempeño del ChatGPT en la resolución de un examen de residencia médica: ¿un indicador de la evolución de inteligencia artificial en educación médica? von Valdez Disla, Alexander, Nouri Kandany, Vahid, Valdez, Pascual

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