Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

Por Burns, Joseph C., Kelly, Michael C., Hoa, Michael, Morell, Robert J., Kelley, Matthew W.
Publicado no Nat Commun (2015)

Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D

Por Lagziel, Ayala, Overlack, Nora, Bernstein, Steven L., Morell, Robert J., Wolfrum, Uwe, Friedman, Thomas B.
Publicado em 2009

A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

Por Mujtaba, Ghulam, Schultz, Julie M, Imtiaz, Ayesha, Morell, Robert J, Friedman, Thomas B, Naz, Sadaf
Publicado no J Med Genet (2015)

Signatures from Tissue-specific MPSS Libraries Identify Transcripts Preferentially Expressed in the Mouse Inner Ear

Por Peters, Linda M., Belyantseva, Inna A., Lagziel, Ayala, Battey, James F., Friedman, Thomas B., Morell, Robert J.
Publicado em 2006

Recessive mutations of TMC1 associated with moderate to severe hearing loss

Por Imtiaz, Ayesha, Maqsood, Azra, Rehman, Atteeq U., Morell, Robert J., Holt, Jeffrey R., Friedman, Thomas B., Naz, Sadaf
Publicado no Neurogenetics (2016)

Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT

Por Griffith, Andrew J., Chowdhry, Aqeel A., Kurima, Kiyoto, Hood, Linda J., Keats, Bronya, Berlin, Charles I., Morell, Robert J., Friedman, Thomas B.
Publicado em 2000

A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction

Por Lee, Sue I., Conrad, Travis, Jones, Sherri M., Lagziel, Ayala, Starost, Matthew F., Belyantseva, Inna A., Friedman, Thomas B., Morell, Robert J.
Publicado em 2013

The Transcription Factors Grainyhead-like 2 and NK2-Homeobox 1 Form a Regulatory Loop That Coordinates Lung Epithelial Cell Morphogenesis and Differentiation

Por Varma, Saaket, Cao, Yuxia, Tagne, Jean-Bosco, Lakshminarayanan, Meenakshi, Li, Jun, Friedman, Thomas B., Morell, Robert J., Warburton, David, Kotton, Darrell N., Ramirez, Maria I.
Publicado em 2012

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Por Ahmed, Zubair M., Riazuddin, Saima, Bernstein, Steve L., Ahmed, Zahoor, Khan, Shaheen, Griffith, Andrew J., Morell, Robert J., Friedman, Thomas B., Riazuddin, Sheikh, Wilcox, Edward R.
Publicado em 2001

DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3

Por Khan, Shahid Yar, Riazuddin, Saima, Shahzad, Mohsin, Ahmed, Nazir, Zafar, Ahmad Usman, Rehman, Atteeq Ur, Morell, Robert J, Griffith, Andrew J, Ahmed, Zubair M, Riazuddin, Sheikh, Friedman, Thomas B
Publicado em 2010

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

Por Rehman, Atteeq Ur, Morell, Robert J., Belyantseva, Inna A., Khan, Shahid Y., Boger, Erich T., Shahzad, Mohsin, Ahmed, Zubair M., Riazuddin, Saima, Khan, Shaheen N., Riazuddin, Sheikh, Friedman, Thomas B.
Publicado em 2010

Molecular architecture underlying fluid absorption by the developing inner ear

Por Honda, Keiji, Kim, Sung Huhn, Kelly, Michael C, Burns, Joseph C, Constance, Laura, Li, Xiangming, Zhou, Fei, Hoa, Michael, Kelley, Matthew W, Wangemann, Philine, Morell, Robert J, Griffith, Andrew J
Publicado no eLife (2017)

Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse

Por Fan, Jianguo, Jia, Li, Li, Yan, Ebrahim, Seham, May-Simera, Helen, Wood, Alynda, Morell, Robert J., Liu, Pinghu, Lei, Jingqi, Kachar, Bechara, Belluscio, Leonardo, Qian, Haohua, Li, Tiansen, Li, Wei, Wistow, Graeme, Dong, Lijin
Publicado no Proc Natl Acad Sci U S A (2017)

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome

Por Faridi, Rabia, Rehman, Atteeq U., Morell, Robert J., Friedman, Penelope L., Demain, Leigh, Zahra, Sana, Khan, Asma Ali, Tohlob, Dalia, Assir, Muhammad Zaman, Beaman, Glenda, Khan, Shaheen N., Newman, William G., Riazuddin, Sheikh, Friedman, Thomas B.
Publicado no Clin Genet (2016)

Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus

Por Naz, Sadaf, Giguere, Chantal M., Kohrman, David C., Mitchem, Kristina L., Riazuddin, Saima, Morell, Robert J., Ramesh, Arabandi, Srisailpathy, Srikumari, Deshmukh, Dilip, Riazuddin, Sheikh, Griffith, Andrew J., Friedman, Thomas B., Smith, Richard J. H., Wilcox, Edward R.
Publicado em 2002

Genetic causes of moderate to severe hearing loss point to modifiers

Por Naz, Sadaf, Imtiaz, Ayesha, Mujtaba, Ghulam, Maqsood, Azra, Bashir, Rasheeda, Bukhari, Ihtisham, Khan, Muhammad R., Ramzan, Memoona, Fatima, Amara, Rehman, Atteeq U., Iqbal, Muddassar, Chaudhry, Taimur, Lund, Merete, Brewer, Carmen C., Morell, Robert J., Friedman, Thomas B.
Publicado no Clin Genet (2016)

Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

Por Ahmed, Zubair M., Morell, Robert J., Riazuddin, Saima, Gropman, Andrea, Shaukat, Shahzad, Ahmad, Mussaber M., Mohiddin, Saidi A., Fananapazir, Lameh, Caruso, Rafael C., Husnain, Tayyab, Khan, Shaheen N., Riazuddin, Sheikh, Griffith, Andrew J., Friedman, Thomas B., Wilcox, Edward R.
Publicado em 2003

Cone Responses in Usher Syndrome Types 1 and 2 by Microvolt Electroretinography

Por Zein, Wadih M., Falsini, Benedetto, Tsilou, Ekaterina T., Turriff, Amy E., Schultz, Julie M., Friedman, Thomas B., Brewer, Carmen C., Zalewski, Christopher K., King, Kelly A., Muskett, Julie A., Rehman, Atteeq U., Morell, Robert J., Griffith, Andrew J., Sieving, Paul A.
Publicado no Invest Ophthalmol Vis Sci (2015)

Heritability of non-speech auditory processing skills

Por Brewer, Carmen C, Zalewski, Christopher K, King, Kelly A, Zobay, Oliver, Riley, Alison, Ferguson, Melanie A, Bird, Jonathan E, McCabe, Margaret M, Hood, Linda J, Drayna, Dennis, Griffith, Andrew J, Morell, Robert J, Friedman, Thomas B, Moore, David R
Publicado no Eur J Hum Genet (2016)

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

Por Ahmed, Zubair M, Cindy Li, Xiaoyan, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward R
Publicado em 2004