Thomas Friedman - Publications

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316 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Miyoshi T, Friedman TB, Watanabe N. Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy. Star Protocols. 2: 100967. PMID 34841279 DOI: 10.1016/j.xpro.2021.100967  1
2021 Adeyemo A, Faridi R, Chattaraj P, Yousaf R, Tona R, Okorie S, Bharadwaj T, Nouel-Saied LM, Acharya A, Schrauwen I, Morell RJ, Leal SM, Friedman TB, Griffith AJ, Roux I. Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European Journal of Human Genetics : Ejhg. PMID 34837038 DOI: 10.1038/s41431-021-00984-w  1
2021 Hochberg I, Demain LAM, Richer J, Thompson K, Urquhart JE, Rea A, Pagarkar W, Rodríguez-Palmero A, Schlüter A, Verdura E, Pujol A, Quijada-Fraile P, Amberger A, Deutschmann AJ, Demetz S, ... ... Friedman TB, et al. Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations. American Journal of Human Genetics. 108: 2195-2204. PMID 34715011 DOI: 10.1016/j.ajhg.2021.10.002  1
2021 Faridi R, Rea A, Fenollar-Ferrer C, O'Keefe RT, Gu S, Munir Z, Khan AA, Riazuddin S, Hoa M, Naz S, Newman WG, Friedman TB. New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human Genetics. PMID 34338890 DOI: 10.1007/s00439-021-02319-7  1
2021 Miyoshi T, Belyantseva IA, Kitajiri SI, Miyajima H, Nishio SY, Usami SI, Kim BJ, Choi BY, Omori K, Shroff H, Friedman TB. Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin cores. Human Genetics. PMID 34232383 DOI: 10.1007/s00439-021-02304-0  1
2021 Miyoshi T, Zhang Q, Miyake T, Watanabe S, Ohnishi H, Chen J, Vishwasrao HD, Chakraborty O, Belyantseva IA, Perrin BJ, Shroff H, Friedman TB, Omori K, Watanabe N. Semi-automated single-molecule microscopy screening of fast-dissociating specific antibodies directly from hybridoma cultures. Cell Reports. 34: 108708. PMID 33535030 DOI: 10.1016/j.celrep.2021.108708  1
2021 Jiang F, Takagi Y, Shams A, Heissler SM, Friedman TB, Sellers JR, Bird JE. The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness. The Journal of Biological Chemistry. 100243. PMID 33428946 DOI: 10.1074/jbc.RA120.014903  1
2021 Alexander CJ, Barzik M, Fujiwara I, Remmert K, Wang YX, Petralia RS, Friedman TB, Hammer JA. Myosin 18Aα targets the guanine nucleotide exchange factor β-Pix to the dendritic spines of cerebellar Purkinje neurons and promotes spine maturation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 35: e21092. PMID 33378124 DOI: 10.1096/fj.202001449R  1
2020 McGrath J, Tung CY, Liao X, Belyantseva IA, Roy P, Chakraborty O, Li J, Berbari NF, Faaborg-Andersen CC, Barzik M, Bird JE, Zhao B, Balakrishnan L, Friedman TB, Perrin BJ. Actin at stereocilia tips is regulated by mechanotransduction and ADF/cofilin. Current Biology : Cb. PMID 33400922 DOI: 10.1016/j.cub.2020.12.006  1
2020 Jiang F, Takagi Y, Shams A, Heissler SM, Friedman TB, Sellers JR, Bird JE. The ATPase mechanism of myosin 15, the molecular motor mutated in DFNB3 human deafness. The Journal of Biological Chemistry. PMID 33372036 DOI: 10.1074/jbc.RA120.014903  1
2020 Wafa TT, Faridi R, King KA, Zalewski C, Yousaf R, Schultz JM, Morell RJ, Muskett J, Turriff A, Tsilo E, Griffith AJ, Friedman TB, Zein WM, Brewer CC. Vestibular Phenotype-Genotype Correlation in a Cohort of 90 Patients with Usher Syndrome. Clinical Genetics. PMID 33089500 DOI: 10.1111/cge.13868  1
2020 Friedman TB, Belyantseva IA, Frolenkov GI. Myosins and Hearing. Advances in Experimental Medicine and Biology. 1239: 317-330. PMID 32451864 DOI: 10.1007/978-3-030-38062-5_13  1
2020 Nolen RM, Hufnagel RB, Friedman TB, Turriff AE, Brewer CC, Zalewski CK, King KA, Wafa TT, Griffith AJ, Brooks BP, Zein WM. Atypical and ultra-rare Usher syndrome: a review. Ophthalmic Genetics. 1-12. PMID 32372680 DOI: 10.1080/13816810.2020.1747090  1
2020 Morell RJ, Olszewski R, Tona R, Leitess S, Wafa TT, Taukulis I, Schultz JM, Thomason EJ, Richards K, Whitley BN, Hill C, Saunders T, Starost MF, Fitzgerald T, Wilson E, ... ... Friedman TB, et al. Noncoding microdeletion in mouse disrupts neural crest migration into the stria vascularis, reduces the endocochlear potential and suggests the neuropathology for human nonsyndromic deafness DFNB39. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32152201 DOI: 10.1523/JNEUROSCI.2278-19.2020  1
2020 Breglio AM, May LA, Barzik M, Welsh NC, Francis SP, Costain TQ, Wang L, Anderson DE, Petralia RS, Wang YX, Friedman TB, Wood MJ, Cunningham LL. Exosomes mediate sensory hair cell protection in the inner ear. The Journal of Clinical Investigation. PMID 32027617 DOI: 10.1172/Jci128867  1
2019 Naz S, Friedman TB. Growth factor and receptor malfunctions associated with human genetic deafness. Clinical Genetics. PMID 31506927 DOI: 10.1111/cge.13641  1
2019 Katsuno T, Belyantseva IA, Cartagena-Rivera AX, Ohta K, Crump SM, Petralia RS, Ono K, Tona R, Imtiaz A, Rehman A, Kiyonari H, Kaneko M, Wang YX, Abe T, Ikeya M, ... ... Friedman TB, et al. TRIOBP-5 sculpts stereocilia rootlets and stiffens supporting cells enabling hearing. Jci Insight. 4. PMID 31217345 DOI: 10.1172/jci.insight.128561  1
2019 Tona R, Chen W, Nakano Y, Reyes LD, Petralia RS, Wang YX, Starost MF, Wafa TT, Morell RJ, Cravedi KD, Hoffmann J, Miyoshi T, Munasinghe JP, Fitzgerald TS, Chudasama Y, ... ... Friedman TB, et al. The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy. Human Molecular Genetics. PMID 30602030 DOI: 10.1093/hmg/ddy445  1
2018 Faridi R, Tona R, Brofferio A, Hoa M, Olszewski R, Schrauwen I, Assir MZK, Bandesha AA, Khan AA, Rehman AU, Brewer C, Ahmed W, Leal SM, Riazuddin S, Boyden SE, ... Friedman TB, et al. Mutational and Phenotypic Spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome. Human Mutation. PMID 30461122 DOI: 10.1002/Humu.23689  1
2018 Richard EM, Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Shahzad M, Acharya A, Khan AA, Imtiaz A, Chakchouk I, Takla C, Abbe I, Rafeeq M, Liaqat K, Chaudhry T, ... ... Friedman TB, et al. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss. Human Mutation. PMID 30303587 DOI: 10.1002/humu.23666  1
2018 Nakano Y, Kelly MC, Rehman AU, Boger ET, Morell RJ, Kelley MW, Friedman TB, Bánfi B. Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness. Cell. PMID 29961578 DOI: 10.1016/J.Cell.2018.06.004  1
2018 Mauriac SA, Hien YE, Bird JE, Carvalho SD, Peyroutou R, Lee SC, Moreau MM, Blanc JM, Gezer A, Medina C, Thoumine O, Beer-Hammer S, Friedman TB, Rüttiger L, Forge A, et al. Author Correction: Defective Gpsm2/Gα signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndrome. Nature Communications. 9: 16188. PMID 29799026 DOI: 10.1038/Ncomms16188  1
2018 Yousaf R, Gu C, Ahmed ZM, Khan SN, Friedman TB, Riazuddin S, Shears SB, Riazuddin S. Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse. Plos Genetics. 14: e1007297. PMID 29590114 DOI: 10.1371/journal.pgen.1007297  1
2018 Ahmed ZM, Jaworek TJ, Sarangdhar GN, Zheng L, Gul K, Khan SN, Friedman TB, Sisk RA, Bartles JR, Riazuddin S, Riazuddin S. Inframe deletion of humanis associated with deafness, vestibulopathy and vision impairment. Journal of Medical Genetics. PMID 29572253 DOI: 10.1136/jmedgenet-2017-105221  1
2018 Melli L, Billington N, Sun SA, Bird JE, Nagy A, Friedman TB, Takagi Y, Sellers JR. Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical properties. Elife. 7. PMID 29419377 DOI: 10.7554/Elife.32871  1
2018 Yousaf R, Ahmed ZM, Giese AP, Morell RJ, Lagziel A, Dabdoub A, Wilcox ER, Riazuddin S, Friedman TB, Riazuddin S. Modifier variant of METTL13 suppresses human GAB1-associated profound deafness. The Journal of Clinical Investigation. PMID 29408807 DOI: 10.1172/JCI97350  1
2018 Melli L, Billington N, Sun SA, Bird JE, Nagy A, Friedman TB, Takagi Y, Sellers JR. Author response: Bipolar filaments of human nonmuscle myosin 2-A and 2-B have distinct motile and mechanical properties Elife. DOI: 10.7554/Elife.32871.046  1
2017 Imtiaz A, Belyantseva IA, Beirl AJ, Fenollar-Ferrer C, Bashir R, Bukhari I, Bouzid A, Shaukat U, Azaiez H, Booth KT, Kahrizi K, Najmabadi H, Maqsood A, Wilson EA, Fitzgerald TS, ... ... Friedman TB, et al. CDC14A Phosphatase is Essential for Hearing and Male Fertility in Mouse and Human. Human Molecular Genetics. PMID 29293958 DOI: 10.1093/hmg/ddx440  1
2017 Chattaraj P, Munjal T, Honda K, Rendtorff ND, Ratay JS, Muskett JA, Risso DS, Roux I, Gertz EM, Schäffer AA, Friedman TB, Morell RJ, Tranebjærg L, Griffith AJ. A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct. Journal of Medical Genetics. PMID 28780564 DOI: 10.1136/jmedgenet-2017-104721  1
2017 Mauriac SA, Hien YE, Bird JE, Carvalho SD, Peyroutou R, Lee SC, Moreau MM, Blanc JM, Geyser A, Medina C, Thoumine O, Beer-Hammer S, Friedman TB, Rüttiger L, Forge A, et al. Defective Gpsm2/Gαi3 signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndrome. Nature Communications. 8: 14907. PMID 28387217 DOI: 10.1038/Ncomms14907  1
2017 Isgrig K, Shteamer JW, Belyantseva IA, Drummond MC, Fitzgerald TS, Vijayakumar S, Jones SM, Griffith AJ, Friedman TB, Cunningham LL, Chien WW. Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 28254438 DOI: 10.1016/J.Ymthe.2017.01.007  1
2016 Bird JE, Barzik M, Drummond MC, Sutton DC, Goodman SM, Morozko EL, Cole SM, Boukhvalova AK, Skidmore J, Syam D, Wilson EA, Fitzgerald T, Rehman AU, Martin DM, Boger ET, ... ... Friedman TB, et al. Harnessing Molecular Motors for Nanoscale Pulldown in Live Cells. Molecular Biology of the Cell. PMID 27932498 DOI: 10.1091/Mbc.E16-08-0583  1
2016 Faridi R, Rehman AU, Morell RJ, Friedman PL, Demain L, Zahra S, Khan AA, Tohlob D, Assir MZ, Beaman G, Khan SN, Newman WG, Riazuddin S, Friedman TB. Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical Genetics. PMID 27629923 DOI: 10.1111/cge.12867  1
2016 Naz S, Imtiaz A, Mujtaba G, Maqsood A, Bashir R, Bukhari I, Khan MR, Ramzan M, Fatima A, Rehman AU, Iqbal M, Chaudhry T, Lund M, Brewer CC, Morell RJ, ... Friedman TB, et al. Genetic causes of moderate to severe hearing loss point to modifiers. Clinical Genetics. PMID 27573290 DOI: 10.1111/cge.12856  1
2016 Rehman AU, Bird JE, Faridi R, Shahzad M, Shah S, Lee K, Khan SN, Imtiaz A, Ahmed ZM, Riazuddin S, Santos-Cortez RL, Ahmad W, Leal SM, Riazuddin S, Friedman TB. Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness. Human Mutation. PMID 27375115 DOI: 10.1002/humu.23042  1
2016 Rehman AU, Friedman TB, Griffith AJ. Unresolved questions regarding human hereditary deafness. Oral Diseases. PMID 27259978 DOI: 10.1111/odi.12516  1
2016 Brewer CC, Zalewski CK, King KA, Zobay O, Riley A, Ferguson MA, Bird JE, McCabe MM, Hood LJ, Drayna D, Griffith AJ, Morell RJ, Friedman TB, Moore DR. Heritability of non-speech auditory processing skills. European Journal of Human Genetics : Ejhg. PMID 26883091 DOI: 10.1038/Ejhg.2015.277  1
2016 Imtiaz A, Maqsood A, Rehman AU, Morell RJ, Holt JR, Friedman TB, Naz S. Recessive mutations of TMC1 associated with moderate to severe hearing loss. Neurogenetics. PMID 26879195 DOI: 10.1007/s10048-016-0477-1  1
2016 Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Ansar M, Wang X, Morell RJ, Isaacson R, Belyantseva IA, Dai H, Acharya A, Qaiser TA, Muhammad D, Ali RA, Shams S, ... ... Friedman TB, et al. Autosomal-Recessive Hearing Impairment due to Rare Missense Variants within S1PR2. American Journal of Human Genetics. PMID 26805784 DOI: 10.1016/J.Ajhg.2015.12.004  1
2015 Friedman T, Michalski M, Goodman TR, Brown JE. 3D printing from diagnostic images: a radiologist's primer with an emphasis on musculoskeletal imaging-putting the 3D printing of pathology into the hands of every physician. Skeletal Radiology. PMID 26592802 DOI: 10.1007/s00256-015-2282-6  1
2015 Weintraub AY, Friedman T, Baumfeld Y, Neuman M, Krissi H. Long term subjective cure rate, urinary tract symptoms and dyspareunia following mesh augmented anterior vaginal wall prolapse repair. International Journal of Surgery (London, England). 24: 33-38. PMID 26525268 DOI: 10.1016/j.ijsu.2015.10.027  1
2015 Chien WW, Isgrig K, Roy S, Belyantseva IA, Drummond MC, May LA, Fitzgerald TS, Friedman TB, Cunningham LL. Gene therapy restores hair cell stereocilia morphology in inner ears of deaf whirler mice. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 26307667 DOI: 10.1038/Mt.2015.150  1
2015 Fang Q, Indzhykulian AA, Mustapha M, Riordan GP, Dolan DF, Friedman TB, Belyantseva IA, Frolenkov GI, Camper SA, Bird JE. The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing. Elife. 4. PMID 26302205 DOI: 10.7554/Elife.08627  1
2015 Buske OJ, Girdea M, Dumitriu S, Gallinger B, Hartley T, Trang H, Misyura A, Friedman T, Beaulieu C, Bone WP, Links AE, Washington NL, Haendel MA, Robinson PN, Boerkoel CF, et al. PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Human Mutation. PMID 26251998 DOI: 10.1002/Humu.22851  1
2015 Mojtahedzadeh M, Lee ML, Friedman TC. Continuation or discontinuation of pioglitazone when starting bedtime insulin in patients with poorly controlled type 2 diabetes in an inner-city population. Journal of Diabetes and Its Complications. PMID 26215435 DOI: 10.1016/j.jdiacomp.2015.06.013  1
2015 Friedman T, Neuman M, Peled Y, Krissi H. A new reusable suturing device for vaginal sacrospinous fixation: feasibility and safety study. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 193: 23-6. PMID 26210292 DOI: 10.1016/j.ejogrb.2015.06.028  1
2015 Hull A, Friedman T, Christianson H, Moore G, Walsh R, Wills B. Risk Acceptance and Desire for Shared Decision Making in Pediatric Computed Tomography Scans: A Survey of 350. Pediatric Emergency Care. 31: 759-61. PMID 26181505 DOI: 10.1097/PEC.0000000000000467  0.01
2015 Wiser I, Parnass AJ, Rachmiel R, Westreich M, Friedman T. Rembrandt's Ocular Pathologies. Ophthalmic Plastic and Reconstructive Surgery. PMID 26125286 DOI: 10.1097/IOP.0000000000000518  1
2015 Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S. A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. Journal of Medical Genetics. 52: 548-52. PMID 25941349 DOI: 10.1136/jmedgenet-2015-103023  1
2015 Drummond MC, Barzik M, Bird JE, Zhang DS, Lechene CP, Corey DP, Cunningham LL, Friedman TB. Live-cell imaging of actin dynamics reveals mechanisms of stereocilia length regulation in the inner ear. Nature Communications. 6: 6873. PMID 25898120 DOI: 10.1038/Ncomms7873  1
2015 Friedman T, Coon D, Kanbour-Shakir A, Michaels J, Rubin JP. Defining the lymphatic system of the anterior abdominal wall: an anatomical study. Plastic and Reconstructive Surgery. 135: 1027-32. PMID 25811569 DOI: 10.1097/PRS.0000000000001136  1
2015 Simon M, Richard EM, Wang X, Shahzad M, Huang VH, Qaiser TA, Potluri P, Mahl SE, Davila A, Nazli S, Hancock S, Yu M, Gargus J, Chang R, Al-Sheqaih N, ... ... Friedman TB, et al. Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. Plos Genetics. 11: e1005097. PMID 25807530 DOI: 10.1016/J.Mito.2015.07.089  1
2015 Oved K, Cohen A, Boico O, Navon R, Friedman T, Etshtein L, Kriger O, Bamberger E, Fonar Y, Yacobov R, Wolchinsky R, Denkberg G, Dotan Y, Hochberg A, Reiter Y, et al. A novel host-proteome signature for distinguishing between acute bacterial and viral infections. Plos One. 10: e0120012. PMID 25785720 DOI: 10.1371/Journal.Pone.0120012  1
2015 Nayak G, Varga L, Trincot C, Shahzad M, Friedman PL, Klimes I, Greinwald JH, Riazuddin SA, Masindova I, Profant M, Khan SN, Friedman TB, Ahmed ZM, Gasperikova D, Riazuddin S, et al. Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Human Genetics. 134: 423-37. PMID 25666562 DOI: 10.1007/s00439-015-1532-y  1
2015 Zein WM, Falsini B, Tsilou ET, Turriff AE, Schultz JM, Friedman TB, Brewer CC, Zalewski CK, King KA, Muskett JA, Rehman AU, Morell RJ, Griffith AJ, Sieving PA. Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography. Investigative Ophthalmology & Visual Science. 56: 107-14. PMID 25425308 DOI: 10.1167/Iovs.14-15355  1
2015 Wang Y, Yan C, Liu L, Wang W, Du H, Fan W, Lutfy K, Jiang M, Friedman TC, Liu Y. 11β-Hydroxysteroid dehydrogenase type 1 shRNA ameliorates glucocorticoid-induced insulin resistance and lipolysis in mouse abdominal adipose tissue. American Journal of Physiology. Endocrinology and Metabolism. 308: E84-95. PMID 25389364 DOI: 10.1152/Ajpendo.00205.2014  1
2015 Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA. ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells. Human Molecular Genetics. 24: 609-24. PMID 25217574 DOI: 10.1093/Hmg/Ddu474  1
2015 Sinha-Hikim I, Duran P, Shen R, Lee M, Friedman TC, Davidson MB. Effect of long term vitamin D supplementation on biomarkers of inflammation in Latino and African-American subjects with pre-diabetes and hypovitaminosis D. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et MéTabolisme. 47: 280-3. PMID 25011019 DOI: 10.1055/s-0034-1383652  1
2015 Fang Q, Indzhykulian AA, Mustapha M, Riordan GP, Dolan DF, Friedman TB, Belyantseva IA, Frolenkov GI, Camper SA, Bird JE. Author response: The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing Elife. DOI: 10.7554/Elife.08627.019  1
2015 Baron L, Boubekeur F, Klacza R, Rahman MY, Scognamiglio C, Kurose N, Friedman T, Fdida S. OneLab: Major computer networking testbeds for IoT and wireless experimentation Proceedings of the Annual International Conference On Mobile Computing and Networking, Mobicom. 2015: 199-200. DOI: 10.1145/2789168.2789180  1
2015 Cicalese D, Joumblatt D, Rossi D, Buob MO, Auge J, Friedman T. A fistful of pings: Accurate and lightweight anycast enumeration and geolocation Proceedings - Ieee Infocom. 26: 2776-2784. DOI: 10.1109/INFOCOM.2015.7218670  1
2015 Baron L, Scognamiglio C, Rahman MY, Klacza R, Cicalese D, Kurose N, Friedman T, Fdida S. OneLab: Major computer networking testbeds open to the IEEE INFOCOM community Proceedings - Ieee Infocom. 2015: 3-4. DOI: 10.1109/INFCOMW.2015.7179314  1
2015 Cicalese D, Auge J, Joumblatt D, Rossi D, Buob MO, Friedman T. Lightweight anycast enumeration and geolocation Proceedings - Ieee Infocom. 2015: 1-2. DOI: 10.1109/INFCOMW.2015.7179313  1
2015 Mazloum R, Augé J, Rossi D, Friedman T. Errors announcing 32-bit ASNs in BGP routes 2015 11th International Conference On the Design of Reliable Communication Networks, Drcn 2015. 87-88. DOI: 10.1109/DRCN.2015.7148991  1
2015 Abbo S, Zezak I, Lev-Yadun S, Shamir O, Friedman T, Gopher A. Harvesting wild flax in the Galilee, Israel and extracting fibers-bearing on Near Eastern plant domestication Israel Journal of Plant Sciences. 62: 52-64. DOI: 10.1080/07929978.2014.907672  1
2014 Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, ... ... Friedman TB, et al. Challenges and solutions for gene identification in the presence of familial locus heterogeneity. European Journal of Human Genetics : Ejhg. PMID 25491636 DOI: 10.1038/Ejhg.2014.266  1
2014 Bird JE, Takagi Y, Billington N, Strub MP, Sellers JR, Friedman TB. Chaperone-enhanced purification of unconventional myosin 15, a molecular motor specialized for stereocilia protein trafficking. Proceedings of the National Academy of Sciences of the United States of America. 111: 12390-5. PMID 25114250 DOI: 10.1073/Pnas.1409459111  1
2014 Fredman R, Wise I, Friedman T, Heller L, Karni T. Skin-sparing mastectomy flap ischemia salvage using urgent hyperbaric chamber oxygen therapy: a case report. Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc. 41: 145-7. PMID 24851552  1
2014 Ivey R, Desai M, Green K, Sinha-Hikim I, Friedman TC, Sinha-Hikim AP. Additive effects of nicotine and high-fat diet on hepatocellular apoptosis in mice: involvement of caspase 2 and inducible nitric oxide synthase-mediated intrinsic pathway signaling. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Mã©Tabolisme. 46: 568-73. PMID 24830635 DOI: 10.1055/s-0034-1375610  1
2014 Hsu-Kim C, Friedman T, Gracely E, Gasperino J. Integrating Palliative Care into Critical Care: A Quality Improvement Study. Journal of Intensive Care Medicine. PMID 24603677 DOI: 10.1177/0885066614523923  1
2014 Spires-Jones TL, Friedman T, Pitstick R, Polydoro M, Roe A, Carlson GA, Hyman BT. Methylene blue does not reverse existing neurofibrillary tangle pathology in the rTg4510 mouse model of tauopathy. Neuroscience Letters. 562: 63-8. PMID 24462887 DOI: 10.1016/J.Neulet.2014.01.013  1
2014 Sinha-Hikim I, Friedman TC, Shin CS, Lee D, Ivey R, Sinha-Hikim AP. Nicotine in combination with a high-fat diet causes intramyocellular mitochondrial abnormalities in male mice. Endocrinology. 155: 865-72. PMID 24424058 DOI: 10.1210/en.2013-1795  1
2014 Rehman AU, Santos-Cortez RL, Morell RJ, Drummond MC, Ito T, Lee K, Khan AA, Basra MA, Wasif N, Ayub M, Ali RA, Raza SI, Nickerson DA, Shendure J, ... ... Friedman TB, et al. Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. American Journal of Human Genetics. 94: 144-52. PMID 24387994 DOI: 10.1016/J.Ajhg.2013.12.004  1
2014 Wang Y, Liu L, Du H, Nagaoka Y, Fan W, Lutfy K, Friedman TC, Jiang M, Liu Y. Transgenic overexpression of hexose-6-phosphate dehydrogenase in adipose tissue causes local glucocorticoid amplification and lipolysis in male mice. American Journal of Physiology. Endocrinology and Metabolism. 306: E543-51. PMID 24381005 DOI: 10.1152/ajpendo.00491.2013  1
2014 Huang G, Basaria S, Travison TG, Ho MH, Davda M, Mazer NA, Miciek R, Knapp PE, Zhang A, Collins L, Ursino M, Appleman E, Dzekov C, Stroh H, Ouellette M, ... ... Friedman T, et al. Testosterone dose-response relationships in hysterectomized women with or without oophorectomy: effects on sexual function, body composition, muscle performance and physical function in a randomized trial. Menopause (New York, N.Y.). 21: 612-23. PMID 24281237 DOI: 10.1097/Gme.0000000000000093  1
2014 O'Dell LE, Natividad LA, Pipkin JA, Roman F, Torres I, Jurado J, Torres OV, Friedman TC, Tenayuca JM, Nazarian A. Enhanced nicotine self-administration and suppressed dopaminergic systems in a rat model of diabetes. Addiction Biology. 19: 1006-19. PMID 23834715 DOI: 10.1111/Adb.12074  1
2014 Augé J, Parmentelat T, Turro N, Avakian S, Baron L, Larabi MA, Rahman MY, Friedman T, Fdida S. Tools to foster a global federation of testbeds Computer Networks. 63: 205-220. DOI: 10.1016/J.Bjp.2013.12.038  1
2014 Casoria P, Rossi D, Augé J, Buob MO, Friedman T, Pescapé A. Distributed active measurement of internet queuing delays Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8362: 278-280. DOI: 10.1007/978-3-319-04918-2-31  1
2014 Mazloum R, Buob MO, Augè J, Baynat B, Rossi D, Friedman T. Violation of interdomain routing assumptions Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8362: 173-182. DOI: 10.1007/978-3-319-04918-2-17  1
2013 Teruya SA, Bazargan-Hejazi S, Mojtahedzadeh M, Doshi M, Russell K, Parker-Kelly D, Friedman TC. A Review of Programs, Components and Outcomes in Biomedical Research Faculty Development. International Journal of University Teaching and Faculty Development. 4: 223-236. PMID 26120379  1
2013 Friedman T, Chen T, Chang A. MRI diagnosis of recurrent pigmented villonodular synovitis following total joint arthroplasty. Hss Journal : the Musculoskeletal Journal of Hospital For Special Surgery. 9: 100-5. PMID 24426852 DOI: 10.1007/s11420-012-9283-y  1
2013 Edwards D, Friedman T, Pearce J. Same admissions tools, different outcomes: a critical perspective on predictive validity in three undergraduate medical schools. Bmc Medical Education. 13: 173. PMID 24373207 DOI: 10.1186/1472-6920-13-173  1
2013 Natividad LA, Torres OV, Friedman TC, O'Dell LE. Adolescence is a period of development characterized by short- and long-term vulnerability to the rewarding effects of nicotine and reduced sensitivity to the anorectic effects of this drug. Behavioural Brain Research. 257: 275-85. PMID 24120402 DOI: 10.1016/J.Bbr.2013.10.003  1
2013 Ren X, Lutfy K, Mangubat M, Ferrini MG, Lee ML, Liu Y, Friedman TC. Alterations in phosphorylated CREB expression in different brain regions following short- and long-term morphine exposure: relationship to food intake. Journal of Obesity. 2013: 764742. PMID 24073333 DOI: 10.1155/2013/764742  1
2013 Chau KH, Friedman T, Tranquilli M, Elefteriades JA. Deep hypothermic circulatory arrest effectively preserves neurocognitive function. The Annals of Thoracic Surgery. 96: 1553-9. PMID 24045075 DOI: 10.1016/j.athoracsur.2013.06.127  1
2013 Liu L, Nagashima K, Yasuda T, Liu Y, Hu HR, He G, Feng B, Zhao M, Zhuang L, Zheng T, Friedman TC, Xiang K. Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes. Diabetologia. 56: 2609-18. PMID 24018988 DOI: 10.1007/s00125-013-3031-9  1
2013 Nie Y, Ferrini MG, Liu Y, Anghel A, Espinosa EV, Stuart RC, Lutfy K, Nillni EA, Friedman TC. Morphine treatment selectively regulates expression of rat pituitary POMC and the prohormone convertases PC1/3 and PC2. Peptides. 47: 99-109. PMID 23891651 DOI: 10.1016/J.Peptides.2013.07.006  1
2013 Indzhykulian AA, Stepanyan R, Nelina A, Spinelli KJ, Ahmed ZM, Belyantseva IA, Friedman TB, Barr-Gillespie PG, Frolenkov GI. Molecular remodeling of tip links underlies mechanosensory regeneration in auditory hair cells. Plos Biology. 11: e1001583. PMID 23776407 DOI: 10.1371/Journal.Pbio.1001583  1
2013 Shahzad M, Sivakumaran TA, Qaiser TA, Schultz JM, Hussain Z, Flanagan M, Bhinder MA, Kissell D, Greinwald JH, Khan SN, Friedman TB, Zhang K, Riazuddin S, Riazuddin S, Ahmed ZM. Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss. Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery. 149: 478-87. PMID 23770805 DOI: 10.1177/0194599813493075  1
2013 Jenkinson EM, Rehman AU, Walsh T, Clayton-Smith J, Lee K, Morell RJ, Drummond MC, Khan SN, Naeem MA, Rauf B, Billington N, Schultz JM, Urquhart JE, Lee MK, Berry A, ... ... Friedman TB, et al. Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease. American Journal of Human Genetics. 92: 605-13. PMID 23541340 DOI: 10.1016/J.Ajhg.2013.02.013  1
2013 Lee SI, Conrad T, Jones SM, Lagziel A, Starost MF, Belyantseva IA, Friedman TB, Morell RJ. A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction. Hearing Research. 300: 1-9. PMID 23528307 DOI: 10.1016/j.heares.2013.02.009  1
2013 Friedman TC. Facing facts: the impact of the face-to-face requirement. Journal of Palliative Medicine. 16: 120-1. PMID 23391398 DOI: 10.1089/jpm.2013.9530  1
2013 Shalom A, Friedman T, Schein O, Hadad E. A novel short-scar breast reduction technique in large breasts. Aesthetic Plastic Surgery. 37: 336-40. PMID 23377144 DOI: 10.1007/s00266-012-9980-4  1
2013 Du H, Liu L, Wang Y, Nakagawa Y, Lyzlov A, Lutfy K, Friedman TC, Peng X, Liu Y. Specific reduction of G6PT may contribute to downregulation of hepatic 11β-HSD1 in diabetic mice. Journal of Molecular Endocrinology. 50: 167-78. PMID 23267038 DOI: 10.1530/Jme-12-0223  1
2013 Bashir ZE, Latief N, Belyantseva IA, Iqbal F, Riazuddin SA, Amer Riazuddin S, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population. Journal of Human Genetics. 58: 102-8. PMID 23235333 DOI: 10.1038/jhg.2012.143  1
2013 Fanning SL, Zilberberg J, Stein J, Vazzana K, Berger SA, Korngold R, Friedman TM. Unraveling graft-versus-host disease and graft-versus-leukemia responses using TCR Vβ spectratype analysis in a murine bone marrow transplantation model. Journal of Immunology (Baltimore, Md. : 1950). 190: 447-57. PMID 23203931 DOI: 10.4049/jimmunol.1201641  1
2013 Friedman T, Miller TT. MR imaging and ultrasound correlation of hip pathologic conditions. Magnetic Resonance Imaging Clinics of North America. 21: 183-94. PMID 23168191 DOI: 10.1016/j.mric.2012.09.002  1
2013 Davidson MB, Duran P, Lee ML, Friedman TC. High-dose vitamin D supplementation in people with prediabetes and hypovitaminosis D. Diabetes Care. 36: 260-6. PMID 23033239 DOI: 10.2337/dc12-1204  1
2013 Chirichella C, Rossi D, Testa C, Friedman T, Pescape A. Passive bufferbloat measurement exploiting transport layer information Globecom - Ieee Global Telecommunications Conference. 2963-2968. DOI: 10.1109/GLOCOM.2013.6831525  1
2013 Edwards D, Coates H, Friedman T. Using aptitude testing to diversify higher education intake - an Australian case study Journal of Higher Education Policy and Management. 35: 136-152. DOI: 10.1080/1360080X.2013.775923  1
2013 Coates H, Meek L, Brown J, Friedman T, Noonan P, Mitchell J. VET leadership for the future - characteristics, contexts and capabilities Journal of Further and Higher Education. 37: 819-843. DOI: 10.1080/0309877X.2012.684042  1
2013 Lee SI, Conrad T, Jones SM, Lagziel A, Starost MF, Belyantseva IA, Friedman TB, Morell RJ. Corrigendum to "A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction" [Hear. Res. 300 (2013) 1-9] Hearing Research. 302: 83. DOI: 10.1016/j.heares.2013.05.008  1
2013 Chirichella C, Rossi D, Testa C, Friedman T, Pescapé A. Remotely gauging upstream bufferbloat delays Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 7799: 250-252. DOI: 10.1007/978-3-642-36516-4-25  1
2013 Bourgeau T, Friedman T. Efficient IP-Level network topology capture Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 7799: 11-20. DOI: 10.1007/978-3-642-36516-4-2  1
2013 Friedman TL. The law still stands Foreign Policy 1
2012 Friedman T, Richman D, Adler R. Sonographically guided cryoneurolysis: preliminary experience and clinical outcomes. Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine. 31: 2025-34. PMID 23197557  1
2012 Friedman T, Lurie DJ, Shalom A. Authentication of Rembrandt's self-portraits through the use of facial aging analysis. The Israel Medical Association Journal : Imaj. 14: 591-4. PMID 23193778  1
2012 Friedman TC, Sinha-Hikim I, Parveen M, Najjar SM, Liu Y, Mangubat M, Shin CS, Lyzlov A, Ivey R, Shaheen M, French SW, Sinha-Hikim AP. Additive effects of nicotine and high-fat diet on hepatic steatosis in male mice. Endocrinology. 153: 5809-20. PMID 23093702 DOI: 10.1210/En.2012-1750  1
2012 Riazuddin S, Belyantseva IA, Giese AP, Lee K, Indzhykulian AA, Nandamuri SP, Yousaf R, Sinha GP, Lee S, Terrell D, Hegde RS, Ali RA, Anwar S, Andrade-Elizondo PB, Sirmaci A, ... ... Friedman TB, et al. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nature Genetics. 44: 1265-71. PMID 23023331 DOI: 10.1038/Ng.2426  1
2012 Varma S, Cao Y, Tagne JB, Lakshminarayanan M, Li J, Friedman TB, Morell RJ, Warburton D, Kotton DN, Ramirez MI. The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiation. The Journal of Biological Chemistry. 287: 37282-95. PMID 22955271 DOI: 10.1074/Jbc.M112.408401  1
2012 Grisaru-Soen G, Friedman T, Dollberg S, Mishali H, Carmeli Y. Late-onset bloodstream infections in preterm infants: a 2-year survey. Pediatrics International : Official Journal of the Japan Pediatric Society. 54: 748-53. PMID 22672070 DOI: 10.1111/j.1442-200X.2012.03679.x  1
2012 Nguyen AT, Marquez P, Hamid A, Kieffer B, Friedman TC, Lutfy K. The rewarding action of acute cocaine is reduced in β-endorphin deficient but not in μ opioid receptor knockout mice. European Journal of Pharmacology. 686: 50-4. PMID 22575525 DOI: 10.1016/J.Ejphar.2012.04.040  1
2012 Tweed JO, Hsia SH, Lutfy K, Friedman TC. The endocrine effects of nicotine and cigarette smoke. Trends in Endocrinology and Metabolism: Tem. 23: 334-42. PMID 22561025 DOI: 10.1016/j.tem.2012.03.006  1
2012 Rachel RA, May-Simera HL, Veleri S, Gotoh N, Choi BY, Murga-Zamalloa C, McIntyre JC, Marek J, Lopez I, Hackett AN, Zhang J, Brooks M, den Hollander AI, Beales PL, Li T, ... ... Friedman TB, et al. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. The Journal of Clinical Investigation. 122: 1233-45. PMID 22446187 DOI: 10.1172/Jci60981  1
2012 Friedman TC, Bloom AM. When death precedes birth: experience of a palliative care team on a labor and delivery unit. Journal of Palliative Medicine. 15: 274-6. PMID 22401354 DOI: 10.1089/jpm.2011.0269  1
2012 Rajavashisth TB, Shaheen M, Norris KC, Pan D, Sinha SK, Ortega J, Friedman TC. Decreased prevalence of diabetes in marijuana users: cross-sectional data from the National Health and Nutrition Examination Survey (NHANES) III. Bmj Open. 2: e000494. PMID 22368296 DOI: 10.1136/bmjopen-2011-000494  1
2012 Ali RA, Rehman AU, Khan SN, Husnain T, Riazuddin S, Friedman TB, Ahmed ZM, Riazuddin S. DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3. Clinical Genetics. 81: 498-500. PMID 22211675 DOI: 10.1111/j.1399-0004.2011.01729.x  1
2012 Zilinsky I, Farber N, Haik J, Weissman O, Friedman T, Winkler E. The hatchet and bilobed flaps revisited: shedding new light on traditional concepts. Journal of Drugs in Dermatology : Jdd. 11: 99-102. PMID 22206084  1
2012 Drummond MC, Belyantseva IA, Friderici KH, Friedman TB. Actin in hair cells and hearing loss. Hearing Research. 288: 89-99. PMID 22200607 DOI: 10.1016/J.Heares.2011.12.003  1
2012 Friedman T, Sehatpour P, Dias E, Perrin M, Javitt DC. Differential relationships of mismatch negativity and visual p1 deficits to premorbid characteristics and functional outcome in schizophrenia. Biological Psychiatry. 71: 521-9. PMID 22192361 DOI: 10.1016/J.Biopsych.2011.10.037  1
2012 Lutfy K, Aimiuwu O, Mangubat M, Shin CS, Nerio N, Gomez R, Liu Y, Friedman TC. Nicotine stimulates secretion of corticosterone via both CRH and AVP receptors. Journal of Neurochemistry. 120: 1108-16. PMID 22191943 DOI: 10.1111/j.1471-4159.2011.07633.x  1
2012 Mangubat M, Lutfy K, Lee ML, Pulido L, Stout D, Davis R, Shin CS, Shahbazian M, Seasholtz S, Sinha-Hikim A, Sinha-Hikim I, O'Dell LE, Lyzlov A, Liu Y, Friedman TC. Effect of nicotine on body composition in mice. The Journal of Endocrinology. 212: 317-26. PMID 22138237 DOI: 10.1530/Joe-11-0350  1
2012 Toubai T, Tawara I, Sun Y, Liu C, Nieves E, Evers R, Friedman T, Korngold R, Reddy P. Induction of acute GVHD by sex-mismatched H-Y antigens in the absence of functional radiosensitive host hematopoietic-derived antigen-presenting cells. Blood. 119: 3844-53. PMID 22101894 DOI: 10.1182/Blood-2011-10-384057  1
2012 Arzumanyan A, Friedman T, Kotei E, Ng IO, Lian Z, Feitelson MA. Epigenetic repression of E-cadherin expression by hepatitis B virus x antigen in liver cancer. Oncogene. 31: 563-72. PMID 21706058 DOI: 10.1038/Onc.2011.255  1
2012 Friedman TW, Yelland GW, Robinson SR. Subtle cognitive impairment in elders with Mini-Mental State Examination scores within the 'normal' range. International Journal of Geriatric Psychiatry. 27: 463-71. PMID 21626569 DOI: 10.1002/Gps.2736  1
2012 Rachel RA, May-Simera HL, Veleri S, Gotoh N, Choi BY, Murga-Zamalloa C, McIntyre JC, Marek J, Lopez I, Hackett AN, Zhang J, Brooks M, Den Hollander AI, Beales PL, Li T, ... ... Friedman TB, et al. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis (Journal of Clinical Investigation (2012) 122, 4, (1233-1245) DOI: 10.1172/JCI60981) Journal of Clinical Investigation. 122: 3025. DOI: 10.1172/Jci65432  1
2012 Bourgeau T, Friedman T. Toward fast and efficient IP-level network topology capture Conext Student 2012 - Proceedings of the Acm Conference On the 2012 Conext Student Workshop. 5-6. DOI: 10.1145/2413247.2413252  1
2012 Chirichella C, Rossi D, Testa C, Friedman T, Pescape A. Inferring the buffering delay of remote BitTorrent peers under LEDBAT vs TCP 2012 Ieee 12th International Conference On Peer-to-Peer Computing, P2p 2012. 77-78. DOI: 10.1109/P2P.2012.6335819  1
2012 Massad-Ivanir N, Friedman T, Nahor A, Eichler S, Bonanno LM, Sa'Ar A, Segal E. Hydrogels synthesized in electrochemically machined porous Si hosts: Effect of nano-scale confinement on polymer properties Soft Matter. 8: 9166-9176. DOI: 10.1039/c2sm25966d  1
2012 Rowley SD, Friedman T, Korngold R. Hematopoietic stem cell transplantation for malignant diseases Clinical Immunology: Principles and Practice: Fourth Edition. 1020-1031. DOI: 10.1016/B978-0-7234-3691-1.00097-0  1
2012 Friedman TJ. "How can Greenville get new industry to come here if we get the label of a C.I.O. Town?": Capital migration and the limits of unionism in the postwar south Life and Labor in the New New South. 16-44.  1
2011 Friedman TC. Vitamin D supplementation to prevent the progression of prediabetes to diabetes: getting closer to a recommendation. Translational Research : the Journal of Laboratory and Clinical Medicine. 158: 273-5. PMID 22005266 DOI: 10.1016/j.trsl.2011.06.007  1
2011 Choi BY, Kim HM, Ito T, Lee KY, Li X, Monahan K, Wen Y, Wilson E, Kurima K, Saunders TL, Petralia RS, Wangemann P, Friedman TB, Griffith AJ. Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition. The Journal of Clinical Investigation. 121: 4516-25. PMID 21965328 DOI: 10.1172/Jci59353  1
2011 Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, ... ... Friedman TB, et al. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. Journal of Medical Genetics. 48: 767-75. PMID 21940737 DOI: 10.1136/jmedgenet-2011-100262  1
2011 Stepanyan RS, Indzhykulian AA, Vélez-Ortega AC, Boger ET, Steyger PS, Friedman TB, Frolenkov GI. TRPA1-mediated accumulation of aminoglycosides in mouse cochlear outer hair cells. Journal of the Association For Research in Otolaryngology : Jaro. 12: 729-40. PMID 21879401 DOI: 10.1007/S10162-011-0288-X  1
2011 Rehman AU, Gul K, Morell RJ, Lee K, Ahmed ZM, Riazuddin S, Ali RA, Shahzad M, Jaleel AU, Andrade PB, Khan SN, Khan S, Brewer CC, Ahmad W, Leal SM, ... ... Friedman TB, et al. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. Human Genetics. 130: 759-65. PMID 21660509 DOI: 10.1007/s00439-011-1018-5  1
2011 Waryah AM, Ahmed ZM, Bhinder MA, Binder MA, Choo DI, Sisk RA, Shahzad M, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Molecular and clinical studies of X-linked deafness among Pakistani families. Journal of Human Genetics. 56: 534-40. PMID 21633365 DOI: 10.1038/jhg.2011.55  1
2011 Simmons CD, Pabona JM, Heard ME, Friedman TM, Spataro MT, Godley AL, Simmen FA, Burnett AF, Simmen RC. Krüppel-like factor 9 loss-of-expression in human endometrial carcinoma links altered expression of growth-regulatory genes with aberrant proliferative response to estrogen. Biology of Reproduction. 85: 378-85. PMID 21543766 DOI: 10.1095/Biolreprod.110.090654  1
2011 Hadad E, Westreich M, Friedman T, Shalom A. Effect of aspirin pre- and postburn on survival of experimental intermediate burns in rats. Journal of Cutaneous Medicine and Surgery. 15: 111-4. PMID 21477559 DOI: 10.2310/7750.2011.10016  1
2011 Arzumanyan A, Friedman T, Ng IO, Clayton MM, Lian Z, Feitelson MA. Does the hepatitis B antigen HBx promote the appearance of liver cancer stem cells? Cancer Research. 71: 3701-8. PMID 21464043 DOI: 10.1158/0008-5472.Can-10-3951  1
2011 Ruth Graham M, Goertzen AL, Girling LG, Friedman T, Pauls RJ, Dickson T, Espenell AE, Mutch WA. Quantitative computed tomography in porcine lung injury with variable versus conventional ventilation: recruitment and surfactant replacement. Critical Care Medicine. 39: 1721-30. PMID 21460711 DOI: 10.1097/Ccm.0B013E3182186D09  1
2011 Friedman TB, Schultz JM, Ahmed ZM, Tsilou ET, Brewer CC. Usher syndrome: hearing loss with vision loss. Advances in Oto-Rhino-Laryngology. 70: 56-65. PMID 21358186 DOI: 10.1159/000322473  1
2011 Riazuddin S, Ahmed ZM, Hegde RS, Khan SN, Nasir I, Shaukat U, Riazuddin S, Butman JA, Griffith AJ, Friedman TB, Choi BY. Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome. Bmc Medical Genetics. 12: 21. PMID 21306635 DOI: 10.1186/1471-2350-12-21  1
2011 Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, ... ... Friedman TB, et al. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. American Journal of Human Genetics. 88: 127-37. PMID 21255762 DOI: 10.1016/J.Ajhg.2010.12.011  1
2011 Ahmed ZM, Yousaf R, Lee BC, Khan SN, Lee S, Lee K, Husnain T, Rehman AU, Bonneux S, Ansar M, Ahmad W, Leal SM, Gladyshev VN, Belyantseva IA, Van Camp G, ... ... Friedman TB, et al. Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74. American Journal of Human Genetics. 88: 19-29. PMID 21185009 DOI: 10.1016/J.Ajhg.2010.11.010  1
2011 Friedman TW, Robinson SR, Yelland GW. Impaired perceptual judgment at low blood alcohol concentrations. Alcohol (Fayetteville, N.Y.). 45: 711-8. PMID 21145695 DOI: 10.1016/J.Alcohol.2010.10.007  1
2011 Wang Y, Nakagawa Y, Liu L, Wang W, Ren X, Anghel A, Lutfy K, Friedman TC, Liu Y. Tissue-specific dysregulation of hexose-6-phosphate dehydrogenase and glucose-6-phosphate transporter production in db/db mice as a model of type 2 diabetes. Diabetologia. 54: 440-50. PMID 21052977 DOI: 10.1007/s00125-010-1956-9  1
2011 Parikh D, Hamid A, Friedman TC, Nguyen K, Tseng A, Marquez P, Lutfy K. Stress-induced analgesia and endogenous opioid peptides: the importance of stress duration. European Journal of Pharmacology. 650: 563-7. PMID 21044625 DOI: 10.1016/j.ejphar.2010.10.050  1
2011 Zilberberg J, Friedman TM, Dranoff G, Korngold R. Treatment with GM-CSF secreting myeloid leukemia cell vaccine prior to autologous-BMT improves the survival of leukemia-challenged mice. Biology of Blood and Marrow Transplantation : Journal of the American Society For Blood and Marrow Transplantation. 17: 330-40. PMID 20946965 DOI: 10.1016/j.bbmt.2010.09.020  1
2011 Baek JI, Park HJ, Park K, Choi SJ, Lee KY, Yi JH, Friedman TB, Drayna D, Shin KS, Kim UK. Pathogenic effects of a novel mutation (c.664_681del) in KCNQ4 channels associated with auditory pathology. Biochimica Et Biophysica Acta. 1812: 536-43. PMID 20832469 DOI: 10.1016/j.bbadis.2010.09.001  1
2011 Augustin B, Friedman T, Teixeira R. Measuring multipath routing in the internet Ieee/Acm Transactions On Networking. 19: 830-840. DOI: 10.1109/Tnet.2010.2096232  1
2011 Friedman T. Current Provision of Psychosocial Care Within Palliative Care Psychosocial Issues in Palliative Care. DOI: 10.1093/acprof:oso/9780199216420.003.0006  1
2011 Friedman T, Gavras A. FIRE OpenLab IP testbed and tool demo Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 6994: 323-324. DOI: 10.1007/978-3-642-24755-2_36  1
2011 Bourgeau T, Augé J, Friedman T. TopHat: Supporting experiments through measurement infrastructure federation Lecture Notes of the Institute For Computer Sciences, Social-Informatics and Telecommunications Engineering, Lnicst. 46: 542-557. DOI: 10.1007/978-3-642-17851-1_41  1
2011 Bird JE, Friedman TB. Regulatory mutations in human hereditary deafness Gene Regulatory Sequences and Human Disease. 137-168. DOI: 10.1007/978-1-4614-1683-8_8  1
2011 Friedman TL, Mandelbaum M. America really was that great Foreign Policy 1
2010 Chen J, Patel R, Friedman TC, Jones KS. The Behavioral and Pharmacological Actions of NMDA Receptor Antagonism are Conserved in Zebrafish Larvae. International Journal of Comparative Psychology / Iscp ; Sponsored by the International Society For Comparative Psychology and the University of Calabria. 23: 82-90. PMID 21278812  0.01
2010 Friedman T. Diagnosing asthma in young children: current research & recommendations. Journal of Pediatric Health Care : Official Publication of National Association of Pediatric Nurse Associates & Practitioners. 24: 305-11. PMID 20804950 DOI: 10.1016/j.pedhc.2009.08.007  1
2010 Friedman TC, Ghods DE, Shahinian HK, Zachery L, Shayesteh N, Seasholtz S, Zuckerbraun E, Lee ML, McCutcheon IE. High prevalence of normal tests assessing hypercortisolism in subjects with mild and episodic Cushing's syndrome suggests that the paradigm for diagnosis and exclusion of Cushing's syndrome requires multiple testing. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Mã©Tabolisme. 42: 874-81. PMID 20803415 DOI: 10.1055/s-0030-1263128  1
2010 Kilimnik G, Kim A, Steiner DF, Friedman TC, Hara M. Intraislet production of GLP-1 by activation of prohormone convertase 1/3 in pancreatic α-cells in mouse models of ß-cell regeneration. Islets. 2: 149-55. PMID 20657753 DOI: 10.4161/Isl.2.3.11396  1
2010 Michaels J, Friedman T, Coon D, Rubin JP. Mons rejuvenation in the massive weight loss patient using superficial fascial system suspension. Plastic and Reconstructive Surgery. 126: 45e-46e. PMID 20595851 DOI: 10.1097/PRS.0b013e3181dab4f7  1
2010 Kitajiri S, Sakamoto T, Belyantseva IA, Goodyear RJ, Stepanyan R, Fujiwara I, Bird JE, Riazuddin S, Riazuddin S, Ahmed ZM, Hinshaw JE, Sellers J, Bartles JR, Hammer JA, Richardson GP, ... ... Friedman TB, et al. Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing. Cell. 141: 786-98. PMID 20510926 DOI: 10.1016/J.Cell.2010.03.049  1
2010 Kingdon D, Afghan S, Arnold R, Faruqui R, Friedman T, Jones I, Jones P, Lloyd K, Nicholls D, O'Neill T, Qurashi I, Ramzan A, Series H, Staufenberg E, Brugha T. A diagnostic system using broad categories with clinically relevant specifiers: lessons for ICD-11. The International Journal of Social Psychiatry. 56: 326-35. PMID 20472661 DOI: 10.1177/0020764010367864  1
2010 Friedman T, O'Brien Coon D, Michaels V J, Bontempo F, Young VL, Clavijo JA, Rubin JP. Hereditary coagulopathies: practical diagnosis and management for the plastic surgeon. Plastic and Reconstructive Surgery. 125: 1544-52. PMID 20440173 DOI: 10.1097/PRS.0b013e3181d51344  1
2010 Hertzano R, Puligilla C, Chan SL, Timothy C, Depireux DA, Ahmed Z, Wolf J, Eisenman DJ, Friedman TB, Riazuddin S, Kelley MW, Strome SE. CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear. Journal of the Association For Research in Otolaryngology : Jaro. 11: 407-18. PMID 20386946 DOI: 10.1007/S10162-010-0211-X  1
2010 Rehman AU, Morell RJ, Belyantseva IA, Khan SY, Boger ET, Shahzad M, Ahmed ZM, Riazuddin S, Khan SN, Riazuddin S, Friedman TB. Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79. American Journal of Human Genetics. 86: 378-88. PMID 20170899 DOI: 10.1016/j.ajhg.2010.01.030  1
2010 Friedman T, O'Brien Coon D, Michaels J, Purnell C, Hur S, Harris DN, Rubin JP. Fleur-de-Lis abdominoplasty: a safe alternative to traditional abdominoplasty for the massive weight loss patient. Plastic and Reconstructive Surgery. 125: 1525-35. PMID 20145584 DOI: 10.1097/PRS.0b013e3181d6e7e0  1
2010 Rosenblatt J, Wu Z, Vasir B, Zarwan C, Stone R, Mills H, Friedman T, Konstantinopoulos PA, Spentzos D, Ghebremichael M, Stevenson K, Neuberg D, Levine JD, Joyce R, Tzachanis D, et al. Generation of tumor-specific T lymphocytes using dendritic cell/tumor fusions and anti-CD3/CD28. Journal of Immunotherapy (Hagerstown, Md. : 1997). 33: 155-66. PMID 20145548 DOI: 10.1097/CJI.0b013e3181bed253  1
2010 Anghel A, Jamieson CA, Ren X, Young J, Porche R, Ozigbo E, Ghods DE, Lee ML, Liu Y, Lutfy K, Friedman TC. Gene expression profiling following short-term and long-term morphine exposure in mice uncovers genes involved in food intake. Neuroscience. 167: 554-66. PMID 20144693 DOI: 10.1016/j.neuroscience.2010.01.043  1
2010 Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, ... ... Friedman TB, et al. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. American Journal of Human Genetics. 86: 148-60. PMID 20137774 DOI: 10.1016/J.Ajhg.2010.01.016  1
2010 Coon D, Michaels J, Gusenoff JA, Purnell C, Friedman T, Rubin JP. Multiple procedures and staging in the massive weight loss population. Plastic and Reconstructive Surgery. 125: 691-8. PMID 20124854 DOI: 10.1097/PRS.0b013e3181c87b3c  1
2010 Vuong C, Van Uum SH, O'Dell LE, Lutfy K, Friedman TC. The effects of opioids and opioid analogs on animal and human endocrine systems. Endocrine Reviews. 31: 98-132. PMID 19903933 DOI: 10.1210/Er.2009-0009  1
2010 Thomson S, Koren G, Fraser LA, Rieder M, Friedman TC, Van Uum SHM. Hair analysis provides a historical record of cortisol levels in cushing's syndrome Experimental and Clinical Endocrinology and Diabetes. 118: 133-138. PMID 19609841 DOI: 10.1055/s-0029-1220771  1
2010 Khan SY, Riazuddin S, Shahzad M, Ahmed N, Zafar AU, Rehman AU, Morell RJ, Griffith AJ, Ahmed ZM, Riazuddin S, Friedman TB. DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3. European Journal of Human Genetics : Ejhg. 18: 125-9. PMID 19603065 DOI: 10.1038/ejhg.2009.121  1
2010 Friedman T. Proposals for a Protestant martyrs' monument at Smithfield Sculpture Journal. 19: 107-112. DOI: 10.3828/sj.2010.8  1
2010 Antoniadis P, Fdida S, Friedman T, Misra V. Federation of virtualized infrastructures: Sharing the value of diversity Proceedings of the 6th International Conference On Emerging Networking Experiments and Technologies, Co-Next'10. DOI: 10.1145/1921168.1921184  1
2010 Claffy K, Aben E, Auge J, Beverly R, Bustamante F, Donnet B, Friedman T, Fomenkov M, Haga P, Luckie M, Shavitt Y. The 2nd Workshop on Active Internet Measurements (AIMS-2) report Sigcomm'10 - Proceedings of the Sigcomm 2010 Conference. 53-58. DOI: 10.1145/1880153.1880162  1
2010 Coates H, Friedman T. Evaluation of the Special Tertiary Admissions Test (STAT) Journal of Higher Education Policy and Management. 32: 117-126. DOI: 10.1080/13600800903575421  1
2010 Donnet B, Baynat B, Friedman T. Improving retouched Bloom filter for trading off selected false positives against false negatives Computer Networks. 54: 3373-3387. DOI: 10.1016/J.Comnet.2010.07.003  1
2010 Fdida S, Friedman T, MacKeith S. OneLab: Developing future internet testbeds Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 6481: 199-200. DOI: 10.1007/978-3-642-17694-4_22  1
2010 Fdida S, Friedman T, Parmentelat T. OneLab: An open federated facility for experimentally driven future internet research Studies in Computational Intelligence. 297: 141-152. DOI: 10.1007/978-3-642-13247-6_7  1
2010 Kilimnik G, Kim A, Steiner DF, Friedman TC, Hara M. Intraislet production of GLP-1 by activation of prohormone convertase 1/3 in pancreatic alpha-cells in mouse models of beta-cell regeneration Islets. 2.  1
2009 Peng AW, Belyantseva IA, Hsu PD, Friedman TB, Heller S. Twinfilin 2 regulates actin filament lengths in cochlear stereocilia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15083-8. PMID 19955359 DOI: 10.1523/Jneurosci.2782-09.2009  1
2009 Afek A, Friedman T, Kugel C, Barshack I, Lurie DJ. Dr. Tulp's Anatomy Lesson by Rembrandt: the third day hypothesis. The Israel Medical Association Journal : Imaj. 11: 389-92. PMID 19911487  1
2009 Friedman T, Golan J, Shalom A, Westreich M. The "Brown sisters": photogrammetric analysis of brow and cheek descent. The Israel Medical Association Journal : Imaj. 11: 470-3. PMID 19891234  1
2009 Lagziel A, Overlack N, Bernstein SL, Morell RJ, Wolfrum U, Friedman TB. Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D. Molecular Vision. 15: 1843-57. PMID 19756182  1
2009 Fanning SL, Appel MY, Berger SA, Korngold R, Friedman TM. The immunological impact of genetic drift in the B10.BR congenic inbred mouse strain. Journal of Immunology (Baltimore, Md. : 1950). 183: 4261-72. PMID 19752227 DOI: 10.4049/jimmunol.0900971  1
2009 Filicko-O'Hara J, Grosso D, Flomenberg PR, Friedman TM, Brunner J, Drobyski W, Ferber A, Kakhniashvili I, Keever-Taylor C, Mookerjee B, Talano JA, Wagner JI, Korngold R, Flomenberg N. Antiviral Responses following L-Leucyl-L-Leucine Methyl Esther (LLME)-Treated Lymphocyte Infusions: Graft-versus-Infection without Graft-versus-Host Disease Biology of Blood and Marrow Transplantation. 15: 1609-1619. PMID 19744572 DOI: 10.1016/J.Bbmt.2009.08.020  1
2009 Waryah AM, Rehman A, Ahmed ZM, Bashir ZH, Khan SY, Zafar AU, Riazuddin S, Friedman TB. DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15 Clinical Genetics. 76: 270-275. PMID 19650862 DOI: 10.1111/j.1399-0004.2009.01209.x  1
2009 Riazuddin S, Anwar S, Fischer M, Ahmed ZM, Khan SY, Janssen AG, Zafar AU, Scholl U, Husnain T, Belyantseva IA, Friedman PL, Riazuddin S, Friedman TB, Fahlke C. Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. American Journal of Human Genetics. 85: 273-80. PMID 19646679 DOI: 10.1016/J.Ajhg.2009.07.003  1
2009 Schultz JM, Khan SN, Ahmed ZM, Riazuddin S, Waryah AM, Chhatre D, Starost MF, Ploplis B, Buckley S, Velásquez D, Kabra M, Lee K, Hassan MJ, Ali G, Ansar M, ... ... Friedman TB, et al. Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39. American Journal of Human Genetics. 85: 25-39. PMID 19576567 DOI: 10.1016/j.ajhg.2009.06.003  1
2009 Belyantseva IA, Perrin BJ, Sonnemann KJ, Zhu M, Stepanyan R, McGee J, Frolenkov GI, Walsh EJ, Friderici KH, Friedman TB, Ervasti JM. Gamma-actin is required for cytoskeletal maintenance but not development. Proceedings of the National Academy of Sciences of the United States of America. 106: 9703-8. PMID 19497859 DOI: 10.1073/Pnas.0900221106  1
2009 Anwar S, Riazuddin S, Ahmed ZM, Tasneem S, Ateeq-ul-Jaleel, Khan SY, Griffith AJ, Friedman TB, Riazuddin S. SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. Journal of Human Genetics. 54: 266-70. PMID 19287372 DOI: 10.1038/jhg.2009.21  1
2009 Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB. Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clinical Genetics. 75: 237-43. PMID 19250381 DOI: 10.1111/j.1399-0004.2008.01128.x  1
2009 Friedman T, Reed M, Elliott AM. The carpal bones in Poland syndrome Skeletal Radiology. 38: 585-591. PMID 19183988 DOI: 10.1007/s00256-008-0638-x  1
2009 Fraser LA, Morrison D, Morley-Forster P, Paul TL, Tokmakejian S, Nicholson RL, Bureau Y, Friedman TC, Van Uum SHM. Oral opioids for chronic non-cancer pain: Higher prevalence of hypogonadism in men than in women Experimental and Clinical Endocrinology and Diabetes. 117: 38-43. PMID 18523930 DOI: 10.1055/s-2008-1076715  1
2009 Ahmed ZM, Riazuddin S, Khan SN, Friedman PL, Friedman TB. USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23 Clinical Genetics. 75: 86-91. PMID 18505454 DOI: 10.1111/j.1399-0004.2008.01038.x  1
2009 Veitch D, Augustin B, Teixeira R, Friedman T. Failure control in multipath route tracing Proceedings - Ieee Infocom. 1395-1403. DOI: 10.1109/INFCOM.2009.5062055  1
2009 Lambert TN, Chavez CA, Hernandez-Sanchez B, Lu P, Bell NS, Ambrosini A, Friedman T, Boyle TJ, Wheeler DR, Huber DL. Synthesis and characterization of titania-graphene nanocomposites Journal of Physical Chemistry C. 113: 19812-19823. DOI: 10.1021/Jp905456F  1
2009 Korngold R, Friedman TM. Murine Models of Graft-versus-Host Disease and Graft-versus-Tumor Effect Thomas' Hematopoietic Cell Transplantation: Stem Cell Transplantation, Fourth Edition. 176-187. DOI: 10.1002/9781444303537.ch14  1
2009 Friedman T. Too large to manage, too big to fail Aba Bank Marketing. 41: 16-17.  1
2009 Friedman TL. Das Energie-internet: Intelligente Autos und Haushaltsgeräte: Eine Reise in die Stadt der Zukunft Internationale Politik. 64: 106-113.  1
2008 Ahmed ZM, Kjellstrom S, Haywood-Watson RJ, Bush RA, Hampton LL, Battey JF, Riazuddin S, Frolenkov G, Sieving PA, Friedman TB. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration. Molecular Vision. 14: 2227-36. PMID 19057657  1
2008 Wohl Y, Aviv A, Friedman T, Barak Y. Cutaneous photodamage in schizophrenia patients Photodermatology Photoimmunology and Photomedicine. 24: 291-295. PMID 19000185 DOI: 10.1111/j.1600-0781.2008.00378.x  1
2008 Ahmed ZM, Masmoudi S, Kalay E, Belyantseva IA, Mosrati MA, Collin RW, Riazuddin S, Hmani-Aifa M, Venselaar H, Kawar MN, Tlili A, van der Zwaag B, Khan SY, Ayadi L, Riazuddin SA, ... ... Friedman TB, et al. Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nature Genetics. 40: 1335-40. PMID 18953341 DOI: 10.1038/ng.245  1
2008 Friedman TL. Green pay dirt. Why strategies to tackle climate change will boost the economy. Scientific American. 299: 25-6. PMID 18847079  0.01
2008 Pall ME, Lao MC, Patel SS, Lee ML, Ghods DE, Chandler DW, Friedman TC. Testosterone and bioavailable testosterone help to distinguish between mild Cushing's syndrome and polycystic ovarian syndrome. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Mã©Tabolisme. 40: 813-8. PMID 18819057 DOI: 10.1055/s-0028-1087186  1
2008 Espinosa VP, Liu Y, Ferrini M, Anghel A, Nie Y, Tripathi PV, Porche R, Jansen E, Stuart RC, Nillni EA, Lutfy K, Friedman TC. Differential regulation of prohormone convertase 1/3, prohormone convertase 2 and phosphorylated cyclic-AMP-response element binding protein by short-term and long-term morphine treatment: implications for understanding the "switch" to opiate addiction. Neuroscience. 156: 788-99. PMID 18771713 DOI: 10.1016/J.Neuroscience.2008.07.063  1
2008 Ahmed ZM, Riazuddin S, Aye S, Ali RA, Venselaar H, Anwar S, Belyantseva PP, Qasim M, Riazuddin S, Friedman TB. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome. Human Genetics. 124: 215-23. PMID 18719945 DOI: 10.1007/s00439-008-0543-3  1
2008 Friedman TM, Goldgirsh K, Berger SA, Zilberberg J, Filicko-O'Hara J, Flomenberg N, Donato M, Rowley SD, Korngold R. Overlap between in vitro donor antihost and in vivo posttransplantation TCR Vβ use: A new paradigm for designer allogeneic blood and marrow transplantation Blood. 112: 3517-3525. PMID 18541718 DOI: 10.1182/blood-2008-03-145391  1
2008 Shalom A, Hadad E, Friedman T, Kremer E, Westreich M. Effect of hyaluronic acid on random-pattern flaps in rats Dermatologic Surgery. 34: 1212-1215. PMID 18513292 DOI: 10.1111/j.1524-4725.2008.34260.x  1
2008 Peters LM, Fridell RA, Boger ET, San Agustin TB, Madeo AC, Griffith AJ, Friedman TB, Morell RJ. A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1. Clinical Genetics. 73: 367-72. PMID 18279434 DOI: 10.1111/j.1399-0004.2008.00966.x  1
2008 Riazuddin S, Nazli S, Ahmed ZM, Yang Y, Zulfiqar F, Shaikh RS, Zafar AU, Khan SN, Sabar F, Javid FT, Wilcox ER, Tsilou E, Boger ET, Sellers JR, Belyantseva IA, ... ... Friedman TB, et al. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Human Mutation. 29: 502-11. PMID 18181211 DOI: 10.1002/Humu.20677  1
2008 Collin RW, Kalay E, Tariq M, Peters T, van der Zwaag B, Venselaar H, Oostrik J, Lee K, Ahmed ZM, Caylan R, Li Y, Spierenburg HA, Eyupoglu E, Heister A, Riazuddin S, ... ... Friedman TB, et al. Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35. American Journal of Human Genetics. 82: 125-38. PMID 18179891 DOI: 10.1016/J.Ajhg.2007.09.008  1
2008 Labay V, Garrido G, Madeo AC, Nance WE, Friedman TB, Friedman PL, Del Castillo I, Griffith AJ. Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss. Clinical Genetics. 73: 50-4. PMID 18028453 DOI: 10.1111/j.1399-0004.2007.00925.x  1
2008 Scheflan M, Gur E, Friedman T. Decision making in breast reconstruction with implants in irradiated patients: An algorithm Innovations in Plastic and Aesthetic Surgery. 311-317. DOI: 10.1007/978-3-540-46326-9_37  1
2008 Friedman TJ. Exploiting the North-South differential: Corporate power, southern politics, and the decline of organized labor after world war II Journal of American History. 95: 323-348.  1
2007 Ain Q, Nazli S, Riazuddin S, Jaleel AU, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3. Human Genetics. 122: 445-50. PMID 17690910 DOI: 10.1007/s00439-007-0418-z  1
2007 Nal N, Ahmed ZM, Erkal E, Alper OM, Lüleci G, Dinç O, Waryah AM, Ain Q, Tasneem S, Husnain T, Chattaraj P, Riazuddin S, Boger E, Ghosh M, Kabra M, ... ... Friedman TB, et al. Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing. Human Mutation. 28: 1014-9. PMID 17546645 DOI: 10.1002/Humu.20556  1
2007 Morell RJ, Brewer CC, Ge D, Snieder H, Zalewski CK, King KA, Drayna D, Friedman TB. A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait. Human Genetics. 122: 103-11. PMID 17533509 DOI: 10.1007/s00439-007-0384-5  1
2007 Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system. The European Journal of Neuroscience. 25: 999-1005. PMID 17331196 DOI: 10.1111/J.1460-9568.2007.05332.X  1
2007 Kono M, Belyantseva IA, Skoura A, Frolenkov GI, Starost MF, Dreier JL, Lidington D, Bolz SS, Friedman TB, Hla T, Proia RL. Deafness and stria vascularis defects in S1P2 receptor-null mice. The Journal of Biological Chemistry. 282: 10690-6. PMID 17284444 DOI: 10.1074/Jbc.M700370200  1
2007 Kitajiri S, Makishima T, Friedman TB, Griffith AJ. A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1. Clinical Genetics. 71: 148-52. PMID 17250663 DOI: 10.1111/j.1399-0004.2007.00739.x  1
2007 Khan SY, Ahmed ZM, Shabbir MI, Kitajiri S, Kalsoom S, Tasneem S, Shayiq S, Ramesh A, Srisailpathy S, Khan SN, Smith RJ, Riazuddin S, Friedman TB, Riazuddin S. Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus. Human Mutation. 28: 417-23. PMID 17226784 DOI: 10.1002/humu.20469  1
2007 Khan SY, Riazuddin S, Tariq M, Anwar S, Shabbir MI, Riazuddin SA, Khan SN, Husnain T, Ahmed ZM, Friedman TB, Riazuddin S. Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3. Human Genetics. 120: 789-93. PMID 17066295 DOI: 10.1007/s00439-006-0275-1  1
2007 Peters LM, Belyantseva IA, Lagziel A, Battey JF, Friedman TB, Morell RJ. Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear. Genomics. 89: 197-206. PMID 17049805 DOI: 10.1016/j.ygeno.2006.09.006  1
2006 Riazuddin S, Ahmed ZM, Fanning AS, Lagziel A, Kitajiri S, Ramzan K, Khan SN, Chattaraj P, Friedman PL, Anderson JM, Belyantseva IA, Forge A, Riazuddin S, Friedman TB. Tricellulin is a tight-junction protein necessary for hearing. American Journal of Human Genetics. 79: 1040-51. PMID 17186462 DOI: 10.1086/510022  1
2006 Stepanyan R, Belyantseva IA, Griffith AJ, Friedman TB, Frolenkov GI. Auditory mechanotransduction in the absence of functional myosin-XVa. The Journal of Physiology. 576: 801-8. PMID 16973713 DOI: 10.1113/jphysiol.2006.118547  1
2006 Ahmed ZM, Goodyear R, Riazuddin S, Lagziel A, Legan PK, Behra M, Burgess SM, Lilley KS, Wilcox ER, Riazuddin S, Griffith AJ, Frolenkov GI, Belyantseva IA, Richardson GP, Friedman TB. The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 7022-34. PMID 16807332 DOI: 10.1523/JNEUROSCI.1163-06.2006  1
2006 Haywood-Watson RJ, Ahmed ZM, Kjellstrom S, Bush RA, Takada Y, Hampton LL, Battey JF, Sieving PA, Friedman TB. Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts. Investigative Ophthalmology & Visual Science. 47: 3074-84. PMID 16799054 DOI: 10.1167/Iovs.06-0108  1
2006 Shabbir MI, Ahmed ZM, Khan SY, Riazuddin S, Waryah AM, Khan SN, Camps RD, Ghosh M, Kabra M, Belyantseva IA, Friedman TB, Riazuddin S. Mutations of human TMHS cause recessively inherited non-syndromic hearing loss. Journal of Medical Genetics. 43: 634-40. PMID 16459341 DOI: 10.1136/jmg.2005.039834  1
2006 Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen K, Naz S, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, ... ... Friedman TB, et al. Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness. American Journal of Human Genetics. 78: 137-43. PMID 16385457 DOI: 10.1086/499164  1
2005 Friedman TB, Schultz JM, Ahmed ZM. Usher syndrome type 1: genotype-phenotype relationships. Retina (Philadelphia, Pa.). 25: S40-S42. PMID 16374329  1
2005 Shaikh RS, Ramzan K, Nazli S, Sattar S, Khan SN, Riazuddin S, Ahmed ZM, Friedman TB, Riazuddin S. A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12. American Journal of Medical Genetics. Part A. 138: 392-5. PMID 16158433 DOI: 10.1002/ajmg.a.30949  1
2005 Lagziel A, Ahmed ZM, Schultz JM, Morell RJ, Belyantseva IA, Friedman TB. Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development. Developmental Biology. 280: 295-306. PMID 15882574 DOI: 10.1016/j.ydbio.2005.01.015  1
2005 Ahmad J, Khan SN, Khan SY, Ramzan K, Riazuddin S, Ahmed ZM, Wilcox ER, Friedman TB, Riazuddin S. DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. Human Genetics. 116: 407-12. PMID 15711797 DOI: 10.1007/s00439-004-1247-y  1
2005 Belyantseva IA, Boger ET, Naz S, Frolenkov GI, Sellers JR, Ahmed ZM, Griffith AJ, Friedman TB. Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia. Nature Cell Biology. 7: 148-56. PMID 15654330 DOI: 10.1038/Ncb1219  1
2005 Ramzan K, Shaikh RS, Ahmad J, Khan SN, Riazuddin S, Ahmed ZM, Friedman TB, Wilcox ER, Riazuddin S. A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1. Human Genetics. 116: 17-22. PMID 15538632 DOI: 10.1007/s00439-004-1205-8  1
2004 Naz S, Griffith AJ, Riazuddin S, Hampton LL, Battey JF, Khan SN, Riazuddin S, Wilcox ER, Friedman TB. Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. Journal of Medical Genetics. 41: 591-5. PMID 15286153 DOI: 10.1136/jmg.2004.018523  1
2004 Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW, Avraham KB. Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene. Human Molecular Genetics. 13: 2143-53. PMID 15254021 DOI: 10.1093/Hmg/Ddh218  1
2004 Frolenkov GI, Belyantseva IA, Friedman TB, Griffith AJ. Genetic insights into the morphogenesis of inner ear hair cells. Nature Reviews. Genetics. 5: 489-98. PMID 15211351 DOI: 10.1038/nrg1377  1
2004 Mohiddin SA, Ahmed ZM, Griffith AJ, Tripodi D, Friedman TB, Fananapazir L, Morell RJ. Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6). Journal of Medical Genetics. 41: 309-14. PMID 15060111 DOI: 10.1136/jmg.2003.011973  1
2004 Brownstein Z, Ben-Yosef T, Dagan O, Frydman M, Abeliovich D, Sagi M, Abraham FA, Taitelbaum-Swead R, Shohat M, Hildesheimer M, Friedman TB, Avraham KB. The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa. Pediatric Research. 55: 995-1000. PMID 15028842 DOI: 10.1203/01.Pdr.0000125258.58267.56  1
2003 Belyantseva IA, Boger ET, Friedman TB. Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle. Proceedings of the National Academy of Sciences of the United States of America. 100: 13958-63. PMID 14610277 DOI: 10.1073/pnas.2334417100  1
2003 Ben-Yosef T, Friedman TB. The genetic bases for syndromic and nonsyndromic deafness among Jews. Trends in Molecular Medicine. 9: 496-502. PMID 14604828  0.01
2003 Belyantseva IA, Labay V, Boger ET, Griffith AJ, Friedman TB. Stereocilia: the long and the short of it. Trends in Molecular Medicine. 9: 458-61. PMID 14604820 DOI: 10.1016/j.molmed.2003.09.008  1
2003 Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabar MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Human Molecular Genetics. 12: 3215-23. PMID 14570705 DOI: 10.1093/Hmg/Ddg358  1
2003 Ness SL, Ben-Yosef T, Bar-Lev A, Madeo AC, Brewer CC, Avraham KB, Kornreich R, Desnick RJ, Willner JP, Friedman TB, Griffith AJ. Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III. Journal of Medical Genetics. 40: 767-72. PMID 14569126 DOI: 10.1136/Jmg.40.10.767  1
2003 Friedman TB, Griffith AJ. Human nonsyndromic sensorineural deafness. Annual Review of Genomics and Human Genetics. 4: 341-402. PMID 14527306 DOI: 10.1146/annurev.genom.4.070802.110347  1
2003 Friedman TB, Schultz JM, Ben-Yosef T, Pryor SP, Lagziel A, Fisher RA, Wilcox ER, Riazuddin S, Ahmed ZM, Belyantseva IA, Griffith AJ. Recent advances in the understanding of syndromic forms of hearing loss. Ear and Hearing. 24: 289-302. PMID 12923420 DOI: 10.1097/01.AUD.0000079804.00047.CE  1
2003 Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, ... ... Friedman TB, et al. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Human Molecular Genetics. 12: 2049-61. PMID 12913076 DOI: 10.1093/Hmg/Ddg210  1
2003 Alford RL, Friedman TB, Keats BJ, Kimberling WJ, Proud VK, Smith RJ, Arnos KS, Korf BR, Rehm HL, Toriello HV. Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 338-41. PMID 12865764 DOI: 10.1097/01.GIM.0000077415.19887.08  1
2003 Pandya A, Arnos KS, Xia XJ, Welch KO, Blanton SH, Friedman TB, Garcia Sanchez G, Liu MD XZ, Morell R, Nance WE. Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 295-303. PMID 12865758 DOI: 10.1097/01.GIM.0000078026.01140.68  1
2003 Naz S, Alasti F, Mowjoodi A, Riazuddin S, Sanati MH, Friedman TB, Griffith AJ, Wilcox ER, Riazuddin S. Distinctive audiometric profile associated with DFNB21 alleles of TECTA. Journal of Medical Genetics. 40: 360-3. PMID 12746400 DOI: 10.1136/jmg.40.5.360  1
2003 Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome. The New England Journal of Medicine. 348: 1664-70. PMID 12711741 DOI: 10.1056/Nejmoa021502  1
2003 Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. Mutations of MYO6 are associated with recessive deafness, DFNB37. American Journal of Human Genetics. 72: 1315-22. PMID 12687499 DOI: 10.1086/375122  1
2002 Riazuddin S, Ahmed ZM, Friedman TB, Griffith AJ, Riazuddin S, Wilcox ER. Genetic modifiers of hereditary hearing loss. Advances in Oto-Rhino-Laryngology. 61: 224-9. PMID 12408088  1
2002 Ahmed ZM, Riazuddin S, Friedman TB, Riazuddin S, Wilcox ER, Griffith AJ. Clinical manifestations of DFNB29 deafness. Advances in Oto-Rhino-Laryngology. 61: 156-60. PMID 12408079  1
2002 Bork JM, Morell RJ, Khan S, Riazuddin S, Wilcox ER, Friedman TB, Griffith AJ. Clinical presentation of DFNB12 and Usher syndrome type 1D. Advances in Oto-Rhino-Laryngology. 61: 145-52. PMID 12408077 DOI: 10.1159/000066829  1
2002 Friedman TB, Hinnant JT, Ghosh M, Boger ET, Riazuddin S, Lupski JR, Potocki L, Wilcox ER. DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation. Advances in Oto-Rhino-Laryngology. 61: 124-30. PMID 12408074 DOI: 10.1159/000066824  1
2002 Peters LM, Anderson DW, Griffith AJ, Grundfast KM, San Agustin TB, Madeo AC, Friedman TB, Morell RJ. Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28. Human Molecular Genetics. 11: 2877-85. PMID 12393799  1
2002 Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus. American Journal of Human Genetics. 71: 632-6. PMID 12145746 DOI: 10.1086/342193  1
2002 Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, Menon PS, Deshmukh D, Griffith AJ, Riazuddin S, Friedman TB, Wilcox ER. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC. Human Genetics. 110: 527-31. PMID 12107438 DOI: 10.1007/s00439-002-0732-4  1
2002 Astuto LM, Bork JM, Weston MD, Askew JW, Fields RR, Orten DJ, Ohliger SJ, Riazuddin S, Morell RJ, Khan S, Riazuddin S, Kremer H, van Hauwe P, Moller CG, Cremers CW, ... ... Friedman TB, et al. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness. American Journal of Human Genetics. 71: 262-75. PMID 12075507 DOI: 10.1086/341558  1
2002 Barber TD, Barber MC, Tomescu O, Barr FG, Ruben S, Friedman TB. Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcoma. Genomics. 79: 278-84. PMID 11863357 DOI: 10.1006/Geno.2002.6703  1
2002 Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nature Genetics. 30: 257-8. PMID 11850623 DOI: 10.1038/Ng848  1
2002 Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, ... ... Friedman TB, et al. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nature Genetics. 30: 277-84. PMID 11850618 DOI: 10.1038/Ng842  1
2002 Griffith AJ, Friedman TB. Auditory function and the M34T allele of connexin 26. Archives of Otolaryngology--Head & Neck Surgery. 128: 94. PMID 11784272  1
2001 Boger ET, Sellers JR, Friedman TB. Human myosin XVBP is a transcribed pseudogene. Journal of Muscle Research and Cell Motility. 22: 477-83. PMID 11964073 DOI: 10.1023/A:1014507705858  1
2001 Lloyd RV, Vidal S, Jin L, Zhang S, Kovacs K, Horvath E, Scheithauer BW, Boger ET, Fridell RA, Friedman TB. Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumors. The American Journal of Pathology. 159: 1375-82. PMID 11583965 DOI: 10.1016/S0002-9440(10)62524-2  1
2001 Wilcox ER, Burton QL, Naz S, Riazuddin S, Smith TN, Ploplis B, Belyantseva I, Ben-Yosef T, Liburd NA, Morell RJ, Kachar B, Wu DK, Griffith AJ, Riazuddin S, Friedman TB. Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. Cell. 104: 165-72. PMID 11163249 DOI: 10.1016/S0092-8674(01)00200-8  1
2001 Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, Polomeno R, Ramesh A, Schloss M, Srisailpathy CR, Wayne S, Bellman S, Desmukh D, Ahmed Z, Khan SN, ... ... Friedman TB, et al. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. American Journal of Human Genetics. 68: 26-37. PMID 11090341 DOI: 10.1086/316954  1
2000 Riazuddin S, Castelein CM, Ahmed ZM, Lalwani AK, Mastroianni MA, Naz S, Smith TN, Liburd NA, Friedman TB, Griffith AJ, Riazuddin S, Wilcox ER. Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nature Genetics. 26: 431-4. PMID 11101839 DOI: 10.1038/82558  1
2000 Friedman T, Battey J, Kachar B, Riazuddin S, Noben-Trauth K, Griffith A, Wilcox E. Modifier genes of hereditary hearing loss. Current Opinion in Neurobiology. 10: 487-93. PMID 10981618 DOI: 10.1016/S0959-4388(00)00120-3  1
2000 Anderson DW, Probst FJ, Belyantseva IA, Fridell RA, Beyer L, Martin DM, Wu D, Kachar B, Friedman TB, Raphael Y, Camper SA. The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells. Human Molecular Genetics. 9: 1729-38. PMID 10915760 DOI: 10.1093/Hmg/9.12.1729  1
2000 Yasunaga S, Grati M, Chardenoux S, Smith TN, Friedman TB, Lalwani AK, Wilcox ER, Petit C. OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. American Journal of Human Genetics. 67: 591-600. PMID 10903124 DOI: 10.1086/303049  1
2000 Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats B, Berlin CI, Morell RJ, Friedman TB. Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT. American Journal of Human Genetics. 67: 745-9. PMID 10903123 DOI: 10.1086/303045  1
2000 Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15. Advances in Oto-Rhino-Laryngology. 56: 131-44. PMID 10868225  1
2000 Pandya A, Oelrich K, Morrell R, Amos KS, Xia XJ, Liu X, Albertorio JR, Blanton SH, Friedman T, Nance WE. Connexin-26 deafness in the United States: Are we ready for the next Millennium? Genetics in Medicine. 2: 64-64. DOI: 10.1097/00125817-200001000-00053  1
1999 Friedman TB, Sellers JR, Avraham KB. Unconventional myosins and the genetics of hearing loss. American Journal of Medical Genetics. 89: 147-57. PMID 10704189 DOI: 10.1002/(Sici)1096-8628(19990924)89:3<147::Aid-Ajmg5>3.0.Co;2-6  1
1999 Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, et al. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics. 61: 243-58. PMID 10552926 DOI: 10.1006/Geno.1999.5976  1
1999 Barber TD, Barber MC, Cloutier TE, Friedman TB. PAX3 gene structure, alternative splicing and evolution Gene. 237: 311-319. PMID 10521655 DOI: 10.1016/S0378-1119(99)00339-X  1
1999 Griffith AJ, Friedman TB. Making sense out of sound. Nature Genetics. 21: 347-9. PMID 10192378 DOI: 10.1038/7668  1
1999 Probst FJ, Chen KS, Zhao Q, Wang A, Friedman TB, Lupski JR, Camper SA. A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2). Genomics. 55: 348-52. PMID 10049592 DOI: 10.1006/Geno.1998.5669  1
1998 Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, Keats B, Friedman TB. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. The New England Journal of Medicine. 339: 1500-5. PMID 9819448 DOI: 10.1056/NEJM199811193392103  1
1998 DeStefano AL, Cupples LA, Arnos KS, Asher JH, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Ramesar RS, et al. Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations. Human Genetics. 102: 499-506. PMID 9654197 DOI: 10.1007/s004390050732  1
1998 Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science (New York, N.Y.). 280: 1447-51. PMID 9603736 DOI: 10.1126/Science.280.5368.1447  1
1998 Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science (New York, N.Y.). 280: 1444-7. PMID 9603735 DOI: 10.1126/Science.280.5368.1444  1
1998 Carey ML, Friedman TB, Asher JH, Innis JW. Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7. Journal of Medical Genetics. 35: 248-50. PMID 9541113 DOI: 10.1136/jmg.35.3.248  0.01
1998 Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, ... ... Friedman TB, et al. Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. American Journal of Human Genetics. 62: 904-15. PMID 9529344 DOI: 10.1086/301786  1
1998 Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science (New York, N.Y.). 279: 1950-4. PMID 9506947 DOI: 10.1126/Science.279.5358.1950  1
1998 Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ER. A mutation in PDS causes non-syndromic recessive deafness. Nature Genetics. 18: 215-7. PMID 9500541 DOI: 10.1038/ng0398-215  1
1997 Innis JW, Asher JH, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia. American Journal of Medical Genetics. 71: 292-7. PMID 9268099 DOI: 10.1002/(Sici)1096-8628(19970822)71:3<292::Aid-Ajmg9>3.0.Co;2-W  1
1997 Morell R, Friedman TB, Asher JH, Robbins LG. The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1). Journal of Medical Genetics. 34: 447-52. PMID 9192262 DOI: 10.1136/jmg.34.6.447  1
1997 Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH. Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA) Human Molecular Genetics. 6: 659-664. PMID 9158138 DOI: 10.1093/HMG/6.5.659  1
1997 Liang Y, Chen H, Asher JH, Chang CC, Friedman TB. Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter. Gene. 184: 163-7. PMID 9031623 DOI: 10.1016/S0378-1119(96)00590-2  1
1997 Morell R, Carey ML, Lalwani AK, Friedman TB, Asher JH. Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1. Human Heredity. 47: 38-41. PMID 9017978 DOI: 10.1159/000154387  1
1996 Asher JH, Harrison RW, Morell R, Carey ML, Friedman TB. Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation. Genomics. 34: 285-98. PMID 8786127 DOI: 10.1006/GENO.1996.0289  1
1996 Asher JH, Sommer A, Morell R, Friedman TB. Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome. Human Mutation. 7: 30-5. PMID 8664898 DOI: 10.1002/(SICI)1098-1004(1996)7:1<30::AID-HUMU4>3.0.CO;2-T  1
1995 Morell R, Liang Y, Asher JH, Weber JL, Hinnant JT, Winata S, Arhya IN, Friedman TB. Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population Human Molecular Genetics. 4: 85-91. PMID 7711738  1
1995 Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17 Nature Genetics. 9: 86-91. PMID 7704031 DOI: 10.1038/Ng0195-86  1
1995 Winata S, Arhya IN, Moeljopawiro S, Hinnant JT, Liang Y, Friedman TB, Asher JH. Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village. Journal of Medical Genetics. 32: 336-43. PMID 7616538 DOI: 10.1136/jmg.32.5.336  1
1994 Carey ML, Liang Y, Barber TD, Morell R, Johnson DH, Cox S, Asher JH, Friedman TB. Dinucleotide repeat polymorphism at D14S542 Human Molecular Genetics. 3: 1712. PMID 7833943 DOI: 10.1093/hmg/3.9.1712-a  1
1993 Barber TD, Morell R, Johnson DH, Asher JH, Friedman TB. A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1 Human Molecular Genetics. 2: 88. PMID 8098246 DOI: 10.1093/Hmg/2.1.88  1
1993 Morell R, Friedman TB, Asher JH. A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family. Human Molecular Genetics. 2: 1487-8. PMID 7902163 DOI: 10.1093/HMG/2.9.1487  1
1992 Wallrath LL, Friedman TB. Combinative oligonucleotide-directed large deletions as a strategy for surveying the regulatory region of a gene. Biotechniques. 12: 214-6. PMID 1616711  1
1992 Friedman TB, Burnett JB, Lootens S, Steinman R, Wallrath LL. The urate oxidase gene of Drosophila pseudoobscura and Drosophila melanogaster: evolutionary changes of sequence and regulation. Journal of Molecular Evolution. 34: 62-77. PMID 1556745  1
1992 Morell R, Friedman TB, Moeljopawiro S, Hartono, Soewito, Asher JH. A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family. Human Molecular Genetics. 1: 243-7. PMID 1303193 DOI: 10.1093/HMG/1.4.243  1
1991 Wallrath LL, Friedman TB. Species differences in the temporal pattern of Drosophila urate oxidase gene expression are attributed to trans-acting regulatory changes. Proceedings of the National Academy of Sciences of the United States of America. 88: 5489-93. PMID 2062830 DOI: 10.1073/pnas.88.13.5489  1
1991 Friedman TB, Owens KN, Burnett JB, Saura AO, Wallrath LL. The faint band/interband region 28C2 to 28C4-5(-) of the Drosophila melanogaster salivary gland polytene chromosomes is rich in transcripts. Molecular & General Genetics : Mgg. 226: 81-7. PMID 1903504 DOI: 10.1007/BF00273590  1
1991 Asher JH, Morell R, Friedman TB. Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPP. Annals of the New York Academy of Sciences. 630: 295-7. PMID 1683205 DOI: 10.1111/J.1749-6632.1991.TB19611.X  1
1990 Asher JH, Friedman TB. Mouse and hamster mutants as models for Waardenburg syndromes in humans. Journal of Medical Genetics. 27: 618-26. PMID 2246770 DOI: 10.1136/jmg.27.10.618  1
1990 Wallrath LL, Burnett JB, Friedman TB. Molecular characterization of the Drosophila melanogaster urate oxidase gene, an ecdysone-repressible gene expressed only in the malpighian tubules. Molecular and Cellular Biology. 10: 5114-27. PMID 2118989  1
1983 Johnson DH, Friedman TB. Purine-resistant Drosophila melanogaster result from mutations in the adenine phosphoribosyltransferase structural gene Proceedings of the National Academy of Sciences of the United States of America. 80: 2990-2994. PMID 6407004 DOI: 10.1073/PNAS.80.10.2990  1
1977 Friedman TB, Johnson DH. Temporal control of urate oxidase activity in drosophila: Evidence of an autonomous timer in malpighian tubules Science. 197: 477-479. PMID 406675 DOI: 10.1126/SCIENCE.406675  1
1973 Friedman TB. Observations on the regulation of uricase activity during development of Drosophila melanogaster Biochemical Genetics. 8: 37-45. PMID 4632615 DOI: 10.1007/BF00485555  1
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