Implementation of a lifestyle and life-skills intervention to prevent weight-gain and cardiometabolic abnormalities in people with first-episode psychosis: the Keeping the Body in Mind program
Curtis, J., Teasdale, S., Morell, R., Wadhwa, P., Lederman, O., Fibbins, H., Watkins, A., Ward, P.
Published in European psychiatry (01.06.2022)
Published in European psychiatry (01.06.2022)
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Journal Article
Genetic causes of moderate to severe hearing loss point to modifiers
Naz, S., Imtiaz, A., Mujtaba, G., Maqsood, A., Bashir, R., Bukhari, I., Khan, M.R., Ramzan, M., Fatima, A., Rehman, A.U., Iqbal, M., Chaudhry, T., Lund, M., Brewer, C.C., Morell, R.J., Friedman, T.B.
Published in Clinical genetics (01.04.2017)
Published in Clinical genetics (01.04.2017)
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Journal Article
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
Faridi, R., Rehman, A.U., Morell, R.J., Friedman, P.L., Demain, L., Zahra, S., Khan, A.A., Tohlob, D., Assir, M.Z., Beaman, G., Khan, S.N., Newman, W.G., Riazuddin, S., Friedman, T.B.
Published in Clinical genetics (01.02.2017)
Published in Clinical genetics (01.02.2017)
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Journal Article
Mutations in the γ-Actin Gene ( ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
Zhu, M., Yang, T., Wei, S., DeWan, A.T., Morell, R.J., Elfenbein, J.L., Fisher, R.A., Leal, S.M., Smith, R. J.H., Friderici, K.H.
Published in American journal of human genetics (01.11.2003)
Published in American journal of human genetics (01.11.2003)
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Journal Article
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
Mohiddin, S A, Ahmed, Z M, Griffith, A J, Tripodi, D, Friedman, T B, Fananapazir, L, Morell, R J
Published in Journal of medical genetics (01.04.2004)
Published in Journal of medical genetics (01.04.2004)
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Journal Article
[Translated article] Results of a preoperative screening and decolonization programme for Staphylococcus aureus in primary hip and knee arthroplasty
Yuste Berenguer, E., Colomina Morales, J., Señor Revuelto, P., Drudis Morell, R., Torra Riera, M., Pilares Ortega, E.P., Trujillano Cabello, J.
Published in Revista española de cirugía ortopédica y traumatología (01.07.2023)
Published in Revista española de cirugía ortopédica y traumatología (01.07.2023)
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Journal Article
CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness
Astuto, L.M., Bork, J.M., Weston, M.D., Askew, J.W., Fields, R.R., Orten, D.J., Ohliger, S.J., Riazuddin, S., Morell, R.J., Khan, S., Riazuddin, S., Kremer, H., van Hauwe, P., Moller, C.G., Cremers, C. W.R.J., Ayuso, C., Heckenlively, J.R., Rohrschneider, K., Spandau, U., Greenberg, J., Ramesar, R., Reardon, W., Bitoun, P., Millan, J., Legge, R., Friedman, T.B., Kimberling, W.J.
Published in American journal of human genetics (01.08.2002)
Published in American journal of human genetics (01.08.2002)
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Journal Article
Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness
Morell, Robert J, Kim, Hung Jeff, Hood, Linda J, Goforth, Leah, Friderici, Karen, Fisher, Rachel, Van Camp, Guy, Berlin, Charles I, Oddoux, Carole, Ostrer, Harry, Keats, Bronya, Friedman, Thomas B, Agustin, Theresa San, Dumon, Jan
Published in The New England journal of medicine (19.11.1998)
Published in The New England journal of medicine (19.11.1998)
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Journal Article
Efficacy and Safety of Simeprevir and Sofosbuvir with and without Ribavirin for 12 Weeks in Subjects with Recurrent Genotype 1 Hepatitis C Post-Orthotopic Liver Transplant: The Galaxy Study
O’Leary, J.G, Brown, K, Burton, J, Firpi-Morell, R, Fontana, R.J, Muir, A, O’Brien, C, Rabinovitz, M, Rajender Reddy, K, Ryan, R, Shprecher, A, Villadiego, S, Prabhakar, A, Brown, R.S
Published in Journal of hepatology (2016)
Published in Journal of hepatology (2016)
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Journal Article
O008 : Efficacy and safety of grazoprevir and elbasvir in hepatitis C genotype 1-infected patients with child–pugh class B cirrhosis (C-salt part A)
Jacobson, I.M, Poordad, F, Firpi-Morell, R, Everson, G.T, Verna, E.C, Bhanja, S, Zhang, B, Caro, L, Wahl, J, Robertson, M, Barr, E, Charles, E.D
Published in Journal of hepatology (01.04.2015)
Published in Journal of hepatology (01.04.2015)
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Journal Article
Correction of Deafness in shaker-2 Mice by an Unconventional Myosin in a BAC Transgene
Probst, Frank J., Fridell, Robert A., Raphael, Yehoash, Saunders, Thomas L., Wang, Aihui, Liang, Yong, Morell, Robert J., Touchman, Jeffrey W., Lyons, Robert H., Noben-Trauth, Konrad, Friedman, Thomas B., Camper, Sally A.
Published in Science (American Association for the Advancement of Science) (29.05.1998)
Published in Science (American Association for the Advancement of Science) (29.05.1998)
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Journal Article
Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3
Wang, Aihui, Liang, Yong, Fridell, Robert A., Probst, Frank J., Wilcox, Edward R., Touchman, Jeffrey W., Morton, Cynthia C., Morell, Robert J., Noben-Trauth, Konrad, Camper, Sally A., Friedman, Thomas B.
Published in Science (American Association for the Advancement of Science) (29.05.1998)
Published in Science (American Association for the Advancement of Science) (29.05.1998)
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Journal Article
Reconsideration of the role of the hippocampus in learned inhibition
Chan, K-H., Morell, Javier R., Jarrard, Leonard E., Davidson, T.L.
Published in Behavioural Brain Research (15.03.2001)
Published in Behavioural Brain Research (15.03.2001)
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Book Review
Journal Article
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1
Peters, LM, Fridell, RA, Boger, ET, San Agustin, TB, Madeo, AC, Griffith, AJ, Friedman, TB, Morell, RJ
Published in Clinical genetics (01.04.2008)
Published in Clinical genetics (01.04.2008)
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Journal Article
Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
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.
Published in American journal of human genetics (01.07.2001)
Published in American journal of human genetics (01.07.2001)
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Journal Article
Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2
Schultz, Julie M, Yang, Yandan, Caride, Ariel J, Filoteo, Adelaida G, Penheiter, Alan R, Lagziel, Ayala, Morell, Robert J, Mohiddin, Saidi A, Fananapazir, Lameh, Madeo, Anne C, Penniston, John T, Griffith, Andrew J
Published in The New England journal of medicine (14.04.2005)
Published in The New England journal of medicine (14.04.2005)
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Journal Article
Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29
Wilcox, Edward R, Burton, Quianna L, Naz, Sadaf, Riazuddin, Saima, Smith, Tenesha N, Ploplis, Barbara, Belyantseva, Inna, Ben-Yosef, Tamar, Liburd, Nikki A, Morell, Robert J, Kachar, Bechara, Wu, Doris K, Griffith, Andrew J, Riazuddin, Sheikh, Friedman, Thomas B
Published in Cell (12.01.2001)
Published in Cell (12.01.2001)
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Journal Article
Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
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.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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Journal Article