Investigating the Contribution of SocioPhysical Structure of Neighborhoods on Residents’ Sense of Attachment von Navid KHALEGHIMOGHADDAM, Sara ARZHANGI, Narges RAJAEIPOUR

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Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients von Mehvari, Sepideh, Karimian Fathi, Nahid, Saki, Sara, Asadnezhad, Maryam, Arzhangi, Sanaz, Ghodratpour, Fatemeh, Mohseni, Marzieh, Zare Ashrafi, Farzane, Sadeghian, Saeed, Boroumand, Mohammadali, Shokohizadeh, Fatemeh, Rostami, Elham, Boroumand, Rahnama, Najafipour, Reza, Malekzadeh, Reza, Riazalhosseini, Yasser, Akbari, Mohammadreza, Lathrop, Mark, Najmabadi, Hossein, Hosseini, Kaveh, Kahrizi, Kimia

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Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum von Taghizadeh, Sara, Vazehan, Raheleh, Beheshtian, Maryam, Sadeghinia, Farnaz, Fattahi, Zohreh, Mohseni, Marzieh, Arzhangi, Sanaz, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein, Kahrizi, Kimia

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Qatar genome: Insights on genomics from the Middle East von Mbarek, Hamdi, Devadoss Gandhi, Geethanjali, Selvaraj, Senthil, Al‐Muftah, Wadha, Badji, Radja, Al‐Sarraj, Yasser, Saad, Chadi, Darwish, Dima, Alvi, Muhammad, Fadl, Tasnim, Yasin, Heba, Alkuwari, Fatima, Razali, Rozaimi, Aamer, Waleed, Abbaszadeh, Fatemeh, Ahmed, Ikhlak, Mokrab, Younes, Suhre, Karsten, Albagha, Omar, Fakhro, Khalid, Badii, Ramin, Ismail, Said I., Althani, Asma

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Precision medicine in hearing loss von Rudman, Jason R., Mei, Christine, Bressler, Sara E., Blanton, Susan H., Liu, Xue-Zhong

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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families von Salime, Sara, Charif, Majida, Bousfiha, Amale, Elrharchi, Soukaina, Bakhchane, Amina, Charoute, Hicham, Kabine, Mostafa, Snoussi, Khalid, Lenaers, Guy, Barakat, Abdelhamid

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Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss von Lenarduzzi, Stefania, Morgan, Anna, Faletra, Flavio, Cappellani, Stefania, Morgutti, Marcello, Mezzavilla, Massimo, Peruzzi, Adelaide, Ghiselli, Sara, Ambrosetti, Umberto, Graziano, Claudio, Seri, Marco, Gasparini, Paolo, Girotto, Giorgia

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A crowdsourcing database for the copy-number variation of the Spanish population von López-López, Daniel, Roldán, Gema, Fernández-Rueda, Jose L, Bostelmann, Gerrit, Carmona, Rosario, Aquino, Virginia, Perez-Florido, Javier, Ortuño, Francisco, Pita, Guillermo, Núñez-Torres, Rocío, González-Neira, Anna, Peña-Chilet, María, Dopazo, Joaquin

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Characterization of the Common Genetic Variation in the Spanish Population of Navarre von Maillo, Alberto, Huergo, Estefania, Apellániz-Ruiz, María, Urrutia-Lafuente, Edurne, Miranda, María, Salgado, Josefa, Pasalodos-Sanchez, Sara, Delgado-Mora, Luna, Teijido, Óscar, Goicoechea, Ibai, Carmona, Rosario, Perez-Florido, Javier, Aquino, Virginia, Lopez-Lopez, Daniel, Peña-Chilet, María, Beltran, Sergi, Dopazo, Joaquín, Lasa, Iñigo, Beloqui, Juan José, Nagen-Scheme, Alonso, Ángel, Gomez-Cabrero, David

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Pathogenetic Insights into Developmental Coordination Disorder Reveal Substantial Overlap with Movement Disorders von Garofalo, Martinica, Vansenne, Fleur, Sival, Deborah A, Verbeek, Dineke S

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Risk of sudden cardiac death in EXOSC5‐related disease von Calame, Daniel G., Herman, Isabella, Fatih, Jawid M., Du, Haowei, Akay, Gulsen, Jhangiani, Shalini N., Coban‐Akdemir, Zeynep, Milewicz, Dianna M., Gibbs, Richard A., Posey, Jennifer E., Marafi, Dana, Hunter, Jill V., Fan, Yuxin, Lupski, James R., Miyake, Christina Y.

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