Anthony P. Monaco, M.D., Ph.D. - Publications

Affiliations: 
President Tufts University, Boston 
Area:
neurodevelopmental disorders, autism, specific language impairment, dyslexia, chorea acanthocytosis and menkes disease
Website:
http://www.ndm.ox.ac.uk/principal-investigators/researcher/anthony-monaco

240 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
2019 Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, ... ... Monaco AP, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77. PMID 30741946 DOI: 10.1038/s41398-019-0402-0  1
2019 Yeshaw WM, van der Zwaag M, Pinto F, Lahaye LL, Faber AI, Gómez-Sánchez R, Dolga AM, Poland C, Monaco AP, van IJzendoorn S, Grzeschik NA, Velayos-Baeza A, Sibon OC. Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility. Elife. 8. PMID 30741634 DOI: 10.7554/eLife.43561  1
2018 Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DVM, Molnár Z. The Neuronal Migration Hypothesis of Dyslexia: A Critical Evaluation Thirty Years On. The European Journal of Neuroscience. PMID 30218584 DOI: 10.1111/ejn.14149  1
2018 Guidi LG, Holloway ZG, Arnoult C, Ray PF, Monaco AP, Molnár Z, Velayos-Baeza A. AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice. Scientific Reports. 8: 10379. PMID 29991750 DOI: 10.1038/s41598-018-28666-6  1
2017 Guidi LG, Mattley J, Martinez-Garay I, Monaco AP, Linden JF, Velayos-Baeza A, Molnár Z. Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing. Cerebral Cortex (New York, N.Y. : 1991). 1-15. PMID 29045729 DOI: 10.1093/cercor/bhx269  1
2017 Franquinho F, Nogueira-Rodrigues J, Duarte JM, Esteves SS, Carter-Su C, Monaco AP, Molnár Z, Velayos-Baeza A, Brites P, Sousa MM. The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling. Cerebral Cortex (New York, N.Y. : 1991). 1-16. PMID 28334068 DOI: 10.1093/cercor/bhx023  1
2016 Martinez-Garay I, Guidi LG, Holloway ZG, Bailey MA, Lyngholm D, Schneider T, Donnison T, Butt SJ, Velayos-Baeza A, Molnár Z, Monaco AP. Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice. Brain Structure & Function. PMID 27510895 DOI: 10.1007/s00429-016-1282-1  1
2016 Mehta ZB, Fine N, Pullen TJ, Cane MC, Hu M, Chabosseau P, Meur G, Velayos-Baeza A, Monaco AP, Marselli L, Marchetti P, Rutter GA. Changes in the expression of the type 2 diabetes-associated gene VPS13C in the β cell are associated with glucose intolerance in humans and mice. American Journal of Physiology. Endocrinology and Metabolism. ajpendo.00074.2016. PMID 27329800 DOI: 10.1152/ajpendo.00074.2016  1
2016 Pettigrew KA, Frinton E, Nudel R, Chan MT, Thompson P, Hayiou-Thomas ME, Talcott JB, Stein J, Monaco AP, Hulme C, Snowling MJ, Newbury DF, Paracchini S. Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. Journal of Neurodevelopmental Disorders. 8: 24. PMID 27307794 DOI: 10.1186/s11689-016-9157-6  0.36
2016 Yang RY, Xue H, Yu L, Velayos-Baeza A, Monaco AP, Liu FT. Identification of VPS13C as a Galectin-12-Binding Protein That Regulates Galectin-12 Protein Stability and Adipogenesis. Plos One. 11: e0153534. PMID 27073999 DOI: 10.1371/journal.pone.0153534  1
2016 Shore R, Covill L, Pettigrew KA, Brandler WM, Diaz R, Xu Y, Tello JA, Talcott JB, Newbury DF, Stein J, Monaco AP, Paracchini S. The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. Human Molecular Genetics. PMID 26908617 DOI: 10.1093/hmg/ddw047  0.36
2015 Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE, Whitehouse AJ, Snowling MJ, et al. Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. Genes, Brain, and Behavior. 14: 369-76. PMID 25778778 DOI: 10.1111/gbb.12213  1
2015 Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC, Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics : Ejhg. PMID 25585696 DOI: 10.1038/ejhg.2014.296  1
2014 Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, ... ... Monaco AP, et al. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments. Plos Genetics. 10: e1004580. PMID 25188300 DOI: 10.1371/journal.pgen.1004580  1
2014 Monaco AP, Morris PJ. Editorial commentary: Increasing focus on antibodies. Transplantation. 98: S1-2. PMID 25093440 DOI: 10.1097/TP.0000000000000266  1
2014 Gialluisi A, Newbury DF, Wilcutt EG, Olson RK, DeFries JC, Brandler WM, Pennington BF, Smith SD, Scerri TS, Simpson NH, Luciano M, Evans DM, Bates TC, Stein JF, ... ... Monaco AP, et al. Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain, and Behavior. 13: 686-701. PMID 25065397 DOI: 10.1111/gbb.12158  1
2014 Monaco AP, Morris PJ. Reverence for the organ donor. Transplantation. 97: 1089. PMID 24804997 DOI: 10.1097/TP.0000000000000195  1
2014 Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Monaco AP, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/j.ajhg.2014.03.018  0.48
2014 Newbury DF, Monaco AP, Paracchini S. Reading and language disorders: the importance of both quantity and quality. Genes. 5: 285-309. PMID 24705331 DOI: 10.3390/genes5020285  1
2014 Monaco AP, Morris PJ. Editors' commentary: the Asian contribution to living donor liver transplantation. Transplantation. 97: S1. PMID 24694463 DOI: 10.1097/TP.0000000000000157  1
2014 Ceroni F, Sagar A, Simpson NH, Gawthrope AJ, Newbury DF, Pinto D, Francis SM, Tessman DC, Cook EH, Monaco AP, Maestrini E, Pagnamenta AT, Jacob S. A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. Autism Research : Official Journal of the International Society For Autism Research. 7: 254-63. PMID 24634087 DOI: 10.1002/aur.1365  1
2014 Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Genes, Brain, and Behavior. 13: 418-29. PMID 24571439 DOI: 10.1111/gbb.12127  1
2014 Morrissey PE, Monaco AP. Donation after circulatory death: current practices, ongoing challenges, and potential improvements. Transplantation. 97: 258-64. PMID 24492420 DOI: 10.1097/01.TP.0000437178.48174.db  1
2014 Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF. Associations of HLA alleles with specific language impairment. Journal of Neurodevelopmental Disorders. 6: 1. PMID 24433325 DOI: 10.1186/1866-1955-6-1  1
2014 Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, et al. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine and Child Neurology. 56: 346-53. PMID 24117048 DOI: 10.1111/dmcn.12294  1
2014 Becker J, Czamara D, Scerri TS, Ramus F, Csépe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygó F, Tóth D, Fauchereau F, Bogliotti C, Iannuzzi S, ... ... Monaco AP, et al. Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. European Journal of Human Genetics : Ejhg. 22: 675-80. PMID 24022301 DOI: 10.1038/ejhg.2013.199  1
2013 Monaco AP. Reflections on the unique tolerogenicity of bone marrow, the enigma of chimerism and clinical tolerance. Clinical Transplants. 157-66. PMID 25095504  1
2013 Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Plos Genetics. 9: e1003751. PMID 24068947 DOI: 10.1371/journal.pgen.1003751  1
2013 Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Monaco AP, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/ng.2711  0.44
2013 Holloway ZG, Velayos-Baeza A, Howell GJ, Levecque C, Ponnambalam S, Sztul E, Monaco AP. Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps. Molecular Biology of the Cell. 24: 1735-48, S1-8. PMID 23596324 DOI: 10.1091/mbc.E12-08-0625  1
2013 Monaco AP. Joseph Edward Murray, M.D., 1919-2012: pioneering transplant and reconstructive plastic surgeon and scientist, nobel Laureate, humanitarian--an appreciation. Transplantation. 95: 903-7. PMID 23429736 DOI: 10.1097/TP.0b013e3182895cf2  1
2013 Newbury DF, Mari F, Sadighi Akha E, Macdermot KD, Canitano R, Monaco AP, Taylor JC, Renieri A, Fisher SE, Knight SJ. Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. European Journal of Human Genetics : Ejhg. 21: 361-5. PMID 22909776 DOI: 10.1038/ejhg.2012.166  1
2012 Scerri TS, Darki F, Newbury DF, Whitehouse AJ, Peyrard-Janvid M, Matsson H, Ang QW, Pennell CE, Ring S, Stein J, Morris AP, Monaco AP, Kere J, Talcott JB, Klingberg T, et al. The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. Plos One. 7: e50321. PMID 23209710 DOI: 10.1371/journal.pone.0050321  1
2012 Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Monaco AP, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/hmg/dds301  0.48
2012 Holt R, Sykes NH, Conceição IC, Cazier JB, Anney RJ, Oliveira G, Gallagher L, Vicente A, Monaco AP, Pagnamenta AT. CNVs leading to fusion transcripts in individuals with autism spectrum disorder. European Journal of Human Genetics : Ejhg. 20: 1141-7. PMID 22549408 DOI: 10.1038/ejhg.2012.73  1
2012 Monaco AP, Morris PJ. Donor disease transmission: minimizing the risks and maximizing the benefits. Transplantation. 93: S1-3. PMID 22374264 DOI: 10.1097/TP.0b013e31824f3d9c  1
2012 Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, ... ... Monaco AP, et al. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. Plos Genetics. 8: e1002521. PMID 22346768 DOI: 10.1371/journal.pgen.1002521  1
2012 Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Monaco AP, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/s00439-011-1094-6  0.64
2011 Velayos-Baeza A, Holinski-Feder E, Neitzel B, Bader B, Critchley EM, Monaco AP, Danek A, Walker RH. Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred. Archives of Neurology. 68: 1330-3. PMID 21987550 DOI: 10.1001/archneurol.2011.239  1
2011 Holt R, Monaco AP. Links between genetics and pathophysiology in the autism spectrum disorders. Embo Molecular Medicine. 3: 438-50. PMID 21805639 DOI: 10.1002/emmm.201100157  1
2011 Monaco AP, Morris PJ. Everolimus and long-term outcomes in renal transplantation: seeking an optimal strategy for immunosuppression. Transplantation. 92: S1-2. PMID 21799391 DOI: 10.1097/TP.0b013e31822a40d7  1
2011 Monaco AP, Morris PJ. Chronic renal allograft damage: not enough immunosuppression? Transplantation. 91: S1-3. PMID 21519212 DOI: 10.1097/TP.0b013e31821b0f24  1
2011 Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P. Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of Neurodevelopmental Disorders. 3: 113-23. PMID 21484201 DOI: 10.1007/s11689-011-9072-9  1
2011 Pagnamenta AT, Holt R, Yusuf M, Pinto D, Wing K, Betancur C, Scherer SW, Volpi EV, Monaco AP. A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3. Journal of Neurodevelopmental Disorders. 3: 124-31. PMID 21484199 DOI: 10.1007/s11689-011-9076-5  1
2011 Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, Monaco AP, Bishop DV, Paracchini S. DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biological Psychiatry. 70: 237-45. PMID 21457949 DOI: 10.1016/j.biopsych.2011.02.005  1
2011 Villanueva P, Newbury DF, Jara L, De Barbieri Z, Mirza G, Palomino HM, Fernández MA, Cazier JB, Monaco AP, Palomino H. Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. European Journal of Human Genetics : Ejhg. 19: 687-95. PMID 21248734 DOI: 10.1038/ejhg.2010.251  1
2011 Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP. Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior Genetics. 41: 90-104. PMID 21165691 DOI: 10.1007/s10519-010-9424-3  1
2011 Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP. PCSK6 is associated with handedness in individuals with dyslexia. Human Molecular Genetics. 20: 608-14. PMID 21051773 DOI: 10.1093/hmg/ddq475  1
2011 Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, ... ... Monaco AP, et al. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of Medical Genetics. 48: 48-54. PMID 20972252 DOI: 10.1136/jmg.2010.079426  1
2011 Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ. Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes, Brain, and Behavior. 10: 158-65. PMID 20846247 DOI: 10.1111/j.1601-183X.2010.00651.x  1
2010 Bradley JA, Hardy M, Neuberger J, Sachs D, Suthanthiran M, Wood K, Monaco AP, Morris PJ. Transplantation: a report of progress. Transplantation. 90: 1245. PMID 21160404 DOI: 10.1097/TP.0b013e3181fdda4e  1
2010 Paracchini S, Monaco AP, Knight JC. An allele-specific gene expression assay to test the functional basis of genetic associations. Journal of Visualized Experiments : Jove. PMID 21085102 DOI: 10.3791/2279  1
2010 Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, Stein J, Smith SD, Pennington BF, Olson RK, DeFries JC, Monaco AP, Richardson AJ. Identification of candidate genes for dyslexia susceptibility on chromosome 18. Plos One. 5: e13712. PMID 21060895 DOI: 10.1371/journal.pone.0013712  1
2010 Newbury DF, Monaco AP. Genetic advances in the study of speech and language disorders. Neuron. 68: 309-20. PMID 20955937 DOI: 10.1016/j.neuron.2010.10.001  1
2010 Velayos-Baeza A, Levecque C, Kobayashi K, Holloway ZG, Monaco AP. The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage. The Journal of Biological Chemistry. 285: 40148-62. PMID 20943657 DOI: 10.1074/jbc.M110.145961  1
2010 Horn D, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco AP, Bonin M, Riess O, Wohlleber E, Illig T, Bezzina CR, et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human Mutation. 31: E1851-60. PMID 20848658 DOI: 10.1002/humu.21362  1
2010 Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, ... ... Monaco AP, et al. Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Science Translational Medicine. 2: 49ra68. PMID 20844286 DOI: 10.1126/scitranslmed.3001267  1
2010 Sousa I, Clark TG, Holt R, Pagnamenta AT, Mulder EJ, Minderaa RB, Bailey AJ, Battaglia A, Klauck SM, Poustka F, Monaco AP. Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Molecular Autism. 1: 7. PMID 20678249 DOI: 10.1186/2040-2392-1-7  1
2010 Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Monaco AP, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/hmg/ddq307  0.64
2010 Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Monaco AP, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/nature09146  0.64
2010 Holt R, Barnby G, Maestrini E, Bacchelli E, Brocklebank D, Sousa I, Mulder EJ, Kantojärvi K, Järvelä I, Klauck SM, Poustka F, Bailey AJ, Monaco AP. Linkage and candidate gene studies of autism spectrum disorders in European populations. European Journal of Human Genetics : Ejhg. 18: 1013-9. PMID 20442744 DOI: 10.1038/ejhg.2010.69  1
2010 Gaber AO, Monaco AP, Russell JA, Lebranchu Y, Mohty M. Rabbit antithymocyte globulin (thymoglobulin): 25 years and new frontiers in solid organ transplantation and haematology. Drugs. 70: 691-732. PMID 20394456 DOI: 10.2165/11315940-000000000-00000  1
2010 Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, ... ... Monaco AP, et al. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological Psychiatry. 68: 320-8. PMID 20346443 DOI: 10.1016/j.biopsych.2010.02.002  1
2010 Addis L, Friederici AD, Kotz SA, Sabisch B, Barry J, Richter N, Ludwig AA, Rübsamen R, Albert FW, Pääbo S, Newbury DF, Monaco AP. A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3. Genes, Brain, and Behavior. 9: 545-61. PMID 20345892 DOI: 10.1111/j.1601-183X.2010.00583.x  1
2010 Newbury DF, Fisher SE, Monaco AP. Recent advances in the genetics of language impairment. Genome Medicine. 2: 6. PMID 20193051 DOI: 10.1186/gm127  1
2010 Morris PJ, Monaco AP. Outcome and allocation of deceased heart-beating donor kidneys in the United kingdom. Transplantation. 89: 371. PMID 20177336 DOI: 10.1097/TP.0b013e3181cb3eac  1
2010 Bodonyi-Kovacs G, Putheti P, Marino M, Avihingsanon Y, Uknis ME, Monaco AP, Strom TB, Pavlakis M. Gene expression profiling of the donor kidney at the time of transplantation predicts clinical outcomes 2 years after transplantation. Human Immunology. 71: 451-5. PMID 20156509 DOI: 10.1016/j.humimm.2010.02.013  1
2010 Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, ... ... Monaco AP, et al. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular Psychiatry. 15: 954-68. PMID 19401682 DOI: 10.1038/mp.2009.34  1
2009 Egbuna OI, Davis RB, Chudinski R, Pavlakis M, Rogers C, Molakatalla P, Johnson SR, Karp S, Monaco AP, Tang H, Hanto DW, Mandelbrot DA. Outcomes with conversion from calcineurin inhibitors to sirolimus after renal transplantation in the context of steroid withdrawal or steroid continuation. Transplantation. 88: 684-92. PMID 19741466 DOI: 10.1097/TP.0b013e3181b27d44  1
2009 Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, ... ... Monaco AP, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American Journal of Human Genetics. 85: 264-72. PMID 19646677 DOI: 10.1016/j.ajhg.2009.07.004  1
2009 Monaco AP, Morris PJ. Editorial commentary: 2007 and 2008 Beaune seminars in transplantation research. Transplantation. 87: S35. PMID 19424001 DOI: 10.1097/TP.0b013e3181a7f020  1
2009 Levecque C, Velayos-Baeza A, Holloway ZG, Monaco AP. The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway. American Journal of Physiology. Cell Physiology. 297: C160-8. PMID 19419997 DOI: 10.1152/ajpcell.00630.2008  1
2009 Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini E, Bailey AJ, Monaco AP. Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European Journal of Human Genetics : Ejhg. 17: 1347-53. PMID 19384346 DOI: 10.1038/ejhg.2009.47  1
2009 Vernes SC, MacDermot KD, Monaco AP, Fisher SE. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European Journal of Human Genetics : Ejhg. 17: 1354-8. PMID 19352412 DOI: 10.1038/ejhg.2009.43  1
2009 Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP. A common variant associated with dyslexia reduces expression of the KIAA0319 gene. Plos Genetics. 5: e1000436. PMID 19325871 DOI: 10.1371/journal.pgen.1000436  1
2009 Newbury DF, Warburton PC, Wilson N, Bacchelli E, Carone S, Lamb JA, Maestrini E, Volpi EV, Mohammed S, Baird G, Monaco AP. Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment. American Journal of Medical Genetics. Part A. 149: 588-97. PMID 19267418 DOI: 10.1002/ajmg.a.32704  1
2009 Asher JE, Lamb JA, Brocklebank D, Cazier JB, Maestrini E, Addis L, Sen M, Baron-Cohen S, Monaco AP. A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12. American Journal of Human Genetics. 84: 279-85. PMID 19200526 DOI: 10.1016/j.ajhg.2009.01.012  1
2009 Monaco AP. The role of mTOR inhibitors in the management of posttransplant malignancy. Transplantation. 87: 157-63. PMID 19155967 DOI: 10.1097/TP.0b013e318193886e  1
2009 Pagnamenta AT, Wing K, Sadighi Akha E, Knight SJ, Bölte S, Schmötzer G, Duketis E, Poustka F, Klauck SM, Poustka A, Ragoussis J, Bailey AJ, Monaco AP. A 15q13.3 microdeletion segregating with autism. European Journal of Human Genetics : Ejhg. 17: 687-92. PMID 19050728 DOI: 10.1038/ejhg.2008.228  1
2009 Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP. MET and autism susceptibility: family and case-control studies. European Journal of Human Genetics : Ejhg. 17: 749-58. PMID 19002214 DOI: 10.1038/ejhg.2008.215  1
2008 Winchester L, Newbury DF, Monaco AP, Ragoussis J. Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays. Cytogenetic and Genome Research. 123: 322-32. PMID 19287171 DOI: 10.1159/000184724  1
2008 Bradley JA, Hardy M, Neuberger J, Sachs D, Suthanthiran M, Wood K, Monaco AP, Morris PJ. Transplantation: a report of progress. Transplantation. 86: 1635. PMID 19104394 DOI: 10.1097/TP.0b013e3181923830  1
2008 Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. A functional genetic link between distinct developmental language disorders. The New England Journal of Medicine. 359: 2337-45. PMID 18987363 DOI: 10.1056/NEJMoa0802828  1
2008 Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, Stein J, Pembrey ME, Ragoussis J, Golding J, Monaco AP. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. The American Journal of Psychiatry. 165: 1576-84. PMID 18829873 DOI: 10.1176/appi.ajp.2008.07121872  1
2008 Morris PJ, Monaco AP. Evidence in transplantation: randomized versus nonrandomized studies. Transplantation. 86: 16-7. PMID 18622270 DOI: 10.1097/TP.0b013e31817d73f0  1
2008 Murphy JE, Vohra RS, Dunn S, Holloway ZG, Monaco AP, Homer-Vanniasinkam S, Walker JH, Ponnambalam S. Oxidised LDL internalisation by the LOX-1 scavenger receptor is dependent on a novel cytoplasmic motif and is regulated by dynamin-2. Journal of Cell Science. 121: 2136-47. PMID 18544637 DOI: 10.1242/jcs.020917  1
2008 Maki T, Carville A, Stillman IE, Sato K, Kodaka T, Minamimura K, Ogawa N, Kanamoto A, Gottschalk R, Monaco AP, Marr-Belvin A, Westmoreland SV, Sehgal P. SV40 infection associated with rituximab treatment after kidney transplantation in nonhuman primates. Transplantation. 85: 893-902. PMID 18360273 DOI: 10.1097/TP.0b013e3181668ecc  1
2008 Velayos-Baeza A, Toma C, Paracchini S, Monaco AP. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human Molecular Genetics. 17: 859-71. PMID 18063668 DOI: 10.1093/hmg/ddm358  1
2008 Falcaro M, Pickles A, Newbury DF, Addis L, Banfield E, Fisher SE, Monaco AP, Simkin Z, Conti-Ramsden G. Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes, Brain, and Behavior. 7: 393-402. PMID 18005161 DOI: 10.1111/j.1601-183X.2007.00364.x  1
2008 Newbury DF, Monaco AP. The application of molecular genetics to the study of developmental language disorder Understanding Developmental Language Disorders: From Theory to Practice. 79-91. DOI: 10.4324/9780203882580  0.01
2008 Velayos-Baeza A, Lévecque C, Dobson-Stone C, Monaco AP. The function of chorein Neuroacanthocytosis Syndromes Ii. 87-105. DOI: 10.1007/978-3-540-71693-8_7  1
2007 Ruiz-Sandoval JL, García-Navarro V, Chiquete E, Dobson-Stone C, Monaco AP, Alvarez-Palazuelos LE, Padilla-Martínez JJ, Barrera-Chairez E, Rodríguez-Figueroa EI, Pérez-García G. Choreoacanthocytosis in a Mexican family. Archives of Neurology. 64: 1661-4. PMID 17998451 DOI: 10.1001/archneur.64.11.1661  1
2007 Morris PJ, Monaco AP, Mulligan J. Instant electronic access to randomized controlled trials (RCT). Transplantation. 84: 939. PMID 17989594 DOI: 10.1097/01.tp.0000280451.92868.76  1
2007 Toma C, Rossi M, Sousa I, Blasi F, Bacchelli E, Alen R, Vanhala R, Monaco AP, Järvelä I, Maestrini E. Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. Molecular Psychiatry. 12: 977-9. PMID 17957233 DOI: 10.1038/sj.mp.4002069  1
2007 Holloway ZG, Grabski R, Szul T, Styers ML, Coventry JA, Monaco AP, Sztul E. Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking. American Journal of Physiology. Cell Physiology. 293: C1753-67. PMID 17913844 DOI: 10.1152/ajpcell.00253.2007  1
2007 Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Alternative splicing in the dyslexia-associated gene KIAA0319. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 627-34. PMID 17846832 DOI: 10.1007/s00335-007-9051-3  1
2007 Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Monaco AP, et al. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry. 12: 1129-39, 1057. PMID 17667961 DOI: 10.1038/sj.mp.4002053  1
2007 Monaco AP, Morris PJ. Editorial comment: a role for alloimmune response mediators in tolerance induction? Transplantation. 84: S1-2. PMID 17632404 DOI: 10.1097/01.tp.0000268483.24959.1b  1
2007 Monaco AP. Is there a rational solution to the kidney shortage? Medicine and Health, Rhode Island. 90: 89-90. PMID 17601289  1
2007 Paracchini S, Scerri T, Monaco AP. The genetic lexicon of dyslexia. Annual Review of Genomics and Human Genetics. 8: 57-79. PMID 17444811 DOI: 10.1146/annurev.genom.8.080706.092312  1
2007 Gautam A, Fischer SA, Yango AF, Gohh RY, Morrissey PE, Monaco AP. Suppression of cell-mediated immunity by a donor-transmitted lymphocytic choriomeningitis virus in a kidney transplant recipient. Transplant Infectious Disease : An Official Journal of the Transplantation Society. 9: 339-42. PMID 17428276 DOI: 10.1111/j.1399-3062.2007.00232.x  1
2007 Monaco AP. Multivariate linkage analysis of specific language impairment (SLI). Annals of Human Genetics. 71: 660-73. PMID 17388790 DOI: 10.1111/j.1469-1809.2007.00361.x  1
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Monaco AP, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/ng1985  0.64
2007 Monaco AP. Reducing the financial disincentives to living kidney donation: will compensation help the way it is supposed to? Nature Clinical Practice. Nephrology. 3: 132-3. PMID 17245328 DOI: 10.1038/ncpneph0399  1
2007 Monaco AP, Morris PJ. Editorial comment: An old drug just keeps getting better: New mechanisms of action suggest new therapeutic targets Transplantation. 84: S1-S2. DOI: 10.1097/01.tp.0000297838.59029.68  1
2007 Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Monaco AP, et al. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells Molecular Psychiatry. 12: 1057. DOI: 10.1038/sj.mp.4002116  1
2006 Morrissey PE, Gautam A, Yang A, Grollman AP, Esparza A, Gohh RY, Monaco AP. Transplantation for Chinese herb nephropathy. Clinical Transplants. 560. PMID 18365433  1
2006 Monaco AP. Introduction of Sir Peter John Morris. Transplantation. 82: 1587-9. PMID 17198240 DOI: 10.1097/01.tp.0000250733.98191.2a  1
2006 Gautam A, Fischer SA, Yango AF, Gohh RY, Morrissey PE, Monaco AP. Cell mediated immunity (CMI) and post transplant viral infections--role of a functional immune assay to titrate immunosuppression. International Immunopharmacology. 6: 2023-6. PMID 17161357 DOI: 10.1016/j.intimp.2006.09.023  1
2006 Lonie L, Porter DE, Fraser M, Cole T, Wise C, Yates L, Wakeling E, Blair E, Morava E, Monaco AP, Ragoussis J. Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases. Human Mutation. 27: 1160. PMID 17041877 DOI: 10.1002/humu.9467  1
2006 Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry. 11: 1085-91, 1061. PMID 17033633 DOI: 10.1038/sj.mp.4001904  1
2006 Howell GJ, Holloway ZG, Cobbold C, Monaco AP, Ponnambalam S. Cell biology of membrane trafficking in human disease. International Review of Cytology. 252: 1-69. PMID 16984815 DOI: 10.1016/S0074-7696(06)52005-4  1
2006 Morrissey PE, Monaco AP. Living kidney donation: evolution and technical aspects of donor nephrectomy. The Surgical Clinics of North America. 86: 1219-35, vii. PMID 16962411 DOI: 10.1016/j.suc.2006.06.008  1
2006 Monaco AP, Morris PJ. Editorial comment: the other consequences of CMV infection. Transplantation. 82: S1-2. PMID 16858267 DOI: 10.1097/01.tp.0000233998.01061.50  1
2006 Gautam A, Morrissey PE, Brem AS, Fischer SA, Gohh RY, Yango AF, Monaco AP. Use of an immune function assay to monitor immunosuppression for treatment of post-transplant lymphoproliferative disorder. Pediatric Transplantation. 10: 613-6. PMID 16856999 DOI: 10.1111/j.1399-3046.2006.00510.x  1
2006 Parr JR, Lamb JA, Bailey AJ, Monaco AP. Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression. Molecular Psychiatry. 11: 617-9; author reply . PMID 16801976 DOI: 10.1038/sj.mp.4001833  1
2006 Yango AF, Gohh RY, Monaco AP, Reinert SE, Gautam A, Dworkin LD, Morrissey PE. Excess risk of renal allograft loss and early mortality among elderly recipients is associated with poor exercise capacity. Clinical Nephrology. 65: 401-7. PMID 16792134  1
2006 Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, ... ... Monaco AP, et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Human Molecular Genetics. 15: 1659-66. PMID 16600991 DOI: 10.1093/hmg/ddl089  1
2006 Monaco AP. Rewards for organ donation: the time has come. Kidney International. 69: 955-7. PMID 16528242 DOI: 10.1038/sj.ki.5000281  1
2006 Grossberg JA, Reinert SE, Monaco AP, Gohh R, Morrissey PE. Utility of a mathematical nomogram to predict delayed graft function: a single-center experience. Transplantation. 81: 155-9. PMID 16436956 DOI: 10.1097/01.tp.0000188621.54448.c8  1
2006 Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. European Journal of Human Genetics : Ejhg. 14: 123-6. PMID 16205742 DOI: 10.1038/sj.ejhg.5201444  1
2006 Monaco AP, Morris PJ. Editorial comment: Heart transplantation, cardiac allograft vasculopathy and proliferation signal inhibitors Transplantation. 82: S1-S2. DOI: 10.1097/01.tp.0000245501.53813.49  1
2006 Monaco AP, Morris PJ. The Fifth Beaune Symposium: Focus on the vascular endothelium in organ transplantation Transplantation. 82: S1-S2. DOI: 10.1097/01.tp.0000231346.64329.75  1
2006 Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia Molecular Psychiatry. 11: 1061. DOI: 10.1038/sj.mp.4001930  1
2006 Flint J, Monaco AP. Focus on behavioural genetics European Journal of Human Genetics. 14: 647-648. DOI: 10.1038/sj.ejhg.5201599  1
2005 Morrissey PE, Dube C, Gohh R, Yango A, Gautam A, Monaco AP. Good samaritan kidney donation. Transplantation. 80: 1369-73. PMID 16340776 DOI: 10.1097/01.tp.0000179153.36227.2d  1
2005 Johnson SR, Pavlakis M, Khwaja K, Karp SJ, Curry M, Curran CC, Monaco AP, Hanto DW. Intensive care unit extubation does not preclude extrarenal organ recovery from donors after cardiac death. Transplantation. 80: 1244-50. PMID 16314792 DOI: 10.1097/01.TP.0000179643.56257.7F  1
2005 Gohh RY, Yango AF, Morrissey PE, Monaco AP, Gautam A, Sharma M, McCarthy ET, Savin VJ. Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipients. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 5: 2907-12. PMID 16303004 DOI: 10.1111/j.1600-6143.2005.01112.x  1
2005 Gautam A, Morrissey PE, Gohh R, Yango A, Monaco AP. Experience with sirolimus for calcineurin minimization/elimination in pancreas-after-kidney transplantation. Transplantation Proceedings. 37: 3542-3. PMID 16298654 DOI: 10.1016/j.transproceed.2005.09.042  1
2005 Newbury DF, Bishop DV, Monaco AP. Genetic influences on language impairment and phonological short-term memory. Trends in Cognitive Sciences. 9: 528-34. PMID 16188486 DOI: 10.1016/j.tics.2005.09.002  1
2005 Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC. Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 46: 1045-56. PMID 16178928 DOI: 10.1111/j.1469-7610.2005.01447.x  1
2005 Johnson SR, Khwaja K, Pavlakis M, Monaco AP, Hanto DW. Older living donors provide excellent quality kidneys: a single center experience (older living donors). Clinical Transplantation. 19: 600-6. PMID 16146550 DOI: 10.1111/j.1399-0012.2004.00328.x  1
2005 Al-Asmi A, Jansen AC, Badhwar A, Dubeau F, Tampieri D, Shustik C, Mercho S, Savard G, Dobson-Stone C, Monaco AP, Andermann F, Andermann E. Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis. Epilepsia. 46: 1256-63. PMID 16060937 DOI: 10.1111/j.1528-1167.2005.65804.x  1
2005 Dobson-Stone C, Velayos-Baeza A, Jansen A, Andermann F, Dubeau F, Robert F, Summers A, Lang AE, Chouinard S, Danek A, Andermann E, Monaco AP. Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis. Neurogenetics. 6: 151-8. PMID 15918062 DOI: 10.1007/s10048-005-0220-9  1
2005 Morris PJ, Monaco AP. Pancreatic islet transplantation: is the glass half-empty or half-full? Transplantation. 79: 1287-8. PMID 15912089 DOI: 10.1097/01.TP.0000161808.41676.3D  1
2005 Avihingsanon Y, Ma N, Pavlakis M, Chon WJ, Uknis ME, Monaco AP, Ferran C, Stillman I, Schachter AD, Mottley C, Zheng XX, Strom TB. On the intraoperative molecular status of renal allografts after vascular reperfusion and clinical outcomes. Journal of the American Society of Nephrology : Jasn. 16: 1542-8. PMID 15888558 DOI: 10.1681/ASN.2005020210  1
2005 Maki T, Gottschalk R, Ogawa N, Monaco AP. Prevention and cure of autoimmune diabetes in nonobese diabetic mice by continuous administration of FTY720. Transplantation. 79: 1051-5. PMID 15880042 DOI: 10.1097/01.TP.0000161220.87548.EE  1
2005 Monaco AP, Morris PJ. Reduction in calcineurin inhibitor exposure and maintenance of effective immunosuppression: clinical experience with everolimus (Certican). Transplantation. 79: S67-8. PMID 15880017  1
2005 MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics. 76: 1074-80. PMID 15877281 DOI: 10.1086/430841  1
2005 Tran MQ, Gohh RY, Morrissey PE, Dworkin LD, Gautam A, Monaco AP, Yango AF. Cryptosporidium infection in renal transplant patients. Clinical Nephrology. 63: 305-9. PMID 15847259  1
2005 Barnby G, Abbott A, Sykes N, Morris A, Weeks DE, Mott R, Lamb J, Bailey AJ, Monaco AP. Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. American Journal of Human Genetics. 76: 950-66. PMID 15830322 DOI: 10.1086/430454  1
2005 Lossos A, Dobson-Stone C, Monaco AP, Soffer D, Rahamim E, Newman JP, Mohiddin S, Fananapazir L, Lerer I, Linetsky E, Reches A, Argov Z, Abramsky O, Gadoth N, Sadeh M, et al. Early clinical heterogeneity in choreoacanthocytosis. Archives of Neurology. 62: 611-4. PMID 15824261 DOI: 10.1001/archneur.62.4.611  1
2005 Monaco AP, Morris PJ. Care of the live kidney donor: consensus on the ultimate gift. Transplantation. 79: S51. PMID 15785360  1
2005 Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E, Blasi F, Maestrini E, Broxholme J, Tzenova J, Weeks D, Bailey AJ, Monaco AP. Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. Journal of Medical Genetics. 42: 132-7. PMID 15689451 DOI: 10.1136/jmg.2004.025668  1
2005 Bonora E, Lamb JA, Barnby G, Sykes N, Moberly T, Beyer KS, Klauck SM, Poustka F, Bacchelli E, Blasi F, Maestrini E, Battaglia A, Haracopos D, Pedersen L, Isager T, ... ... Monaco AP, et al. Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. European Journal of Human Genetics : Ejhg. 13: 198-207. PMID 15523497 DOI: 10.1038/sj.ejhg.5201315  1
2005 Monaco AP, Morris PJ. Editorial comment: 10 Years and getting better Transplantation. 80: S175-S176. DOI: 10.1097/00007890-200510151-00001  1
2005 Dobson-Stone C, Rampoldi L, Monaco AP. The spectrum of mutations and possible function of the CHAC Gene Neuroacanthocytosis Syndromes. 169-175. DOI: 10.1007/1-4020-2898-9_19  1
2005 Monaco AP, Morris PJ. B cells and alloantibodies in tolerance: A new look Transplantation. 79: S1-S2.  1
2004 Monaco AP. The beginning of clinical tolerance in solid organ allografts. Experimental and Clinical Transplantation : Official Journal of the Middle East Society For Organ Transplantation. 2: 153-61. PMID 15859922  1
2004 Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Journal of Medical Genetics. 41: 853-7. PMID 15520411 DOI: 10.1136/jmg.2004.018341  1
2004 Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics. 75: 1046-58. PMID 15514892 DOI: 10.1086/426404  1
2004 Morris PJ, Monaco AP. Ethical issues and xenotransplantation. Transplantation. 78: 1099-100. PMID 15502701 DOI: 10.1097/01.TP.0000146577.84256.07  1
2004 Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP. Analysis of the human VPS13 gene family. Genomics. 84: 536-49. PMID 15498460 DOI: 10.1016/j.ygeno.2004.04.012  1
2004 Porter DE, Lonie L, Fraser M, Dobson-Stone C, Porter JR, Monaco AP, Simpson AH. Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study. The Journal of Bone and Joint Surgery. British Volume. 86: 1041-6. PMID 15446535 DOI: 10.1302/0301-620X.86B7.14815  1
2004 Kanamoto A, Monaco AP, Maki T. Active role of chimerism in transplantation tolerance induced by antilymphocyte serum, sirolimus, and bone-marrow-cell infusion. Transplantation. 78: 825-30. PMID 15385800 DOI: 10.1097/01.TP.0000135463.21290.6B  1
2004 Dobson-Stone C, Velayos-Baeza A, Filippone LA, Westbury S, Storch A, Erdmann T, Wroe SJ, Leenders KL, Lang AE, Dotti MT, Federico A, Mohiddin SA, Fananapazir L, Daniels G, Danek A, ... Monaco AP, et al. Chorein detection for the diagnosis of chorea-acanthocytosis. Annals of Neurology. 56: 299-302. PMID 15293285 DOI: 10.1002/ana.20200  1
2004 Morrissey PE, Gautam A, Amaral JF, Monaco AP. Keeping up with the Jones's: open donor nephrectomy in the laparoscopic era. Transplantation Proceedings. 36: 1285-7. PMID 15251313 DOI: 10.1016/j.transproceed.2004.05.075  1
2004 Monaco AP. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment American Journal of Human Genetics. 74: 1225-1238. PMID 15133743 DOI: 10.1086/421529  1
2004 Morris PJ, Monaco AP. HLA in the allocation of cadaver kidneys: a global perspective. Transplantation. 77: 608. PMID 15084945 DOI: 10.1097/01.TP.0000105322.23279.59  1
2004 Morrissey PE, Gohh R, Yango A, Gautam A, Monaco AP. Renal transplant survival from older donors: a single center experience. Archives of Surgery (Chicago, Ill. : 1960). 139: 384-9; discussion 38. PMID 15078705 DOI: 10.1001/archsurg.139.4.384  1
2004 Monaco AP, Morris PJ. Clinical Tolerance: the end of the beginning. Transplantation. 77: 921-5. PMID 15077038 DOI: 10.1097/01.TP.0000123232.14907.F2  1
2004 Monaco AP. Prospects and strategies for clinical tolerance. Transplantation Proceedings. 36: 227-31. PMID 15013353 DOI: 10.1016/j.transproceed.2003.11.047  1
2004 Morris PJ, Monaco AP. A meta-analysis from the Cochrane Library reviewing interleukin 2 receptor antagonists in renal transplantation. Transplantation. 77: 165. PMID 14742975 DOI: 10.1097/01.TP.0000112919.54256.8D  1
2004 Morris PJ, Monaco AP. Regulatory T cells finally get the attention they deserve. Transplantation. 77: S2-3. PMID 14726757  1
2004 Cobbold C, Coventry J, Ponnambalam S, Monaco AP. Actin and microtubule regulation of trans-Golgi network architecture, and copper-dependent protein transport to the cell surface. Molecular Membrane Biology. 21: 59-66. PMID 14668139 DOI: 10.1080/096870310001607350  1
2004 Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects. Molecular Psychiatry. 9: 485-93. PMID 14625563 DOI: 10.1038/sj.mp.4001450  1
2004 Morris PJ, Monaco AP. Facial transplantation: Is the time right? Transplantation. 77: 329. DOI: 10.1097/01.TP.0000117797.90116.F2  1
2004 Morris PJ, Monaco AP. Kidney transplantation in patients with abnormal bladders Transplantation. 77: 1111. DOI: 10.1097/01.TP.0000116757.19214.8D  1
2004 Morris PJ, Monaco AP. Organ donation: Altruism or self interest? Transplantation. 77: 149. DOI: 10.1097/01.TP.0000105321.34723.9A  1
2004 Monaco AP, Morris PJ. The costs and benefits of organ procurement: How much is a year of quality life worth? Transplantation. 78: 1703. DOI: 10.1097/00007890-200412270-00001  1
2004 Morris PJ, Monaco AP. Detecting medication non-compliance: Electronic devices or candid patients? Transplantation. 77: 767. DOI: 10.1097/00007890-200403150-00024  1
2003 Morris PJ, Monaco AP. Tolerance comes of age. Editorial comment. Transplantation. 76: 1407-8. PMID 14657673 DOI: 10.1097/01.TP.0000100815.95097.8E  1
2003 Morris PJ, Monaco AP. Geographic disparities in access to organ transplantation. Transplantation. 76: 1383. PMID 14627920 DOI: 10.1097/01.TP.0000090280.25184.6F  1
2003 Cobbold C, Monaco AP, Sivaprasadarao A, Ponnambalam S. Aberrant trafficking of transmembrane proteins in human disease. Trends in Cell Biology. 13: 639-47. PMID 14624842 DOI: 10.1016/j.tcb.2003.10.008  1
2003 Francks C, Fisher SE, Marlow AJ, MacPhie IL, Taylor KE, Richardson AJ, Stein JF, Monaco AP. Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American Journal of Psychiatry. 160: 1970-7. PMID 14594743 DOI: 10.1176/appi.ajp.160.11.1970  1
2003 Bacchelli E, Blasi F, Biondolillo M, Lamb JA, Bonora E, Barnby G, Parr J, Beyer KS, Klauck SM, Poustka A, Bailey AJ, Monaco AP, Maestrini E. Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Molecular Psychiatry. 8: 916-24. PMID 14593429 DOI: 10.1038/sj.mp.4001340  1
2003 Francks C, DeLisi LE, Shaw SH, Fisher SE, Richardson AJ, Stein JF, Monaco AP. Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human Molecular Genetics. 12: 3225-30. PMID 14583442 DOI: 10.1093/hmg/ddg362  1
2003 Barnby G, Monaco AP. Strategies for autism candidate gene analysis. Novartis Foundation Symposium. 251: 48-63; discussion 63. PMID 14521187  1
2003 Bonora E, Beyer KS, Lamb JA, Parr JR, Klauck SM, Benner A, Paolucci M, Abbott A, Ragoussis I, Poustka A, Bailey AJ, Monaco AP. Analysis of reelin as a candidate gene for autism. Molecular Psychiatry. 8: 885-92. PMID 14515139 DOI: 10.1038/sj.mp.4001310  1
2003 Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a Journal of Neurology. 126: 2455-62. PMID 12876151 DOI: 10.1093/brain/awg247  1
2003 Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C, Cantor RM, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American Journal of Human Genetics. 72: 1268-79. PMID 12687500 DOI: 10.1086/375139  1
2003 Bohlega S, Al-Jishi A, Dobson-Stone C, Rampoldi L, Saha P, Murad H, Kareem A, Roberts G, Monaco AP. Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 403-7. PMID 12671946 DOI: 10.1002/mds.10361  0.68
2003 Francks C, DeLisi LE, Fisher SE, Laval SH, Rue JE, Stein JF, Monaco AP. Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American Journal of Human Genetics. 72: 499-502. PMID 12596796 DOI: 10.1086/367548  1
2003 Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ, Talcott JB, Stein JF, Monaco AP, Cardon LR. Use of multivariate linkage analysis for dissection of a complex cognitive trait. American Journal of Human Genetics. 72: 561-70. PMID 12587094 DOI: 10.1086/368201  1
2003 Fisher SE, Lai CS, Monaco AP. Deciphering the genetic basis of speech and language disorders. Annual Review of Neuroscience. 26: 57-80. PMID 12524432 DOI: 10.1146/annurev.neuro.26.041002.131144  1
2003 Morris PJ, Monaco AP. Ambulatory blood pressure monitoring in renal transplantation Transplantation. 76: 1638. DOI: 10.1097/01.TP.0000092002.19290.48  1
2002 Francks C, MacPhie IL, Monaco AP. The genetic basis of dyslexia. The Lancet. Neurology. 1: 483-90. PMID 12849333  0.56
2002 Newbury DF, Monaco AP. Talking genes - the molecular basis of language impairment. Biologist (London, England). 49: 255-60. PMID 12486301  0.64
2002 Newbury DF, Monaco AP. Molecular genetics of speech and language disorders. Current Opinion in Pediatrics. 14: 696-701. PMID 12436038  0.64
2002 Dobson-Stone C, Danek A, Rampoldi L, Hardie RJ, Chalmers RM, Wood NW, Bohlega S, Dotti MT, Federico A, Shizuka M, Tanaka M, Watanabe M, Ikeda Y, Brin M, Goldfarb LG, ... ... Monaco AP, et al. Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. European Journal of Human Genetics : Ejhg. 10: 773-81. PMID 12404112 DOI: 10.1038/sj.ejhg.5200866  1
2002 Lamb JA, Parr JR, Bailey AJ, Monaco AP. Autism: in search of susceptibility genes. Neuromolecular Medicine. 2: 11-28. PMID 12230302 DOI: 10.1385/NMM:2:1:11  0.52
2002 Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature. 418: 869-72. PMID 12192408 DOI: 10.1038/nature01025  1
2002 Smalley SL, Kustanovich V, Minassian SL, Stone JL, Ogdie MN, McGough JJ, McCracken JT, MacPhie IL, Francks C, Fisher SE, Cantor RM, Monaco AP, Nelson SF. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American Journal of Human Genetics. 71: 959-63. PMID 12187510 DOI: 10.1086/342732  0.64
2002 Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American Journal of Human Genetics. 70: 1183-96. PMID 11923911 DOI: 10.1086/340112  0.64
2002 Bonora E, Bacchelli E, Levy ER, Blasi F, Marlow A, Monaco AP, Maestrini E. Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. Molecular Psychiatry. 7: 289-301. PMID 11920156 DOI: 10.1038/sj.mp.4001004  1
2002 Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP. Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric Genetics. 12: 35-41. PMID 11901358 DOI: 10.1097/00041444-200203000-00005  1
2002 Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP. FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics. 70: 1318-27. PMID 11894222 DOI: 10.1086/339931  1
2002 Dobson-Stone C, Fairclough R, Dunne E, Brown J, Dissanayake M, Munro CS, Strachan T, Burge S, Sudbrak R, Monaco AP, Hovnanian A. Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene. The Journal of Investigative Dermatology. 118: 338-43. PMID 11841554 DOI: 10.1046/j.0022-202x.2001.01675.x  1
2002 Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP. A genomewide linkage screen for relative hand skill in sibling pairs. American Journal of Human Genetics. 70: 800-5. PMID 11774074 DOI: 10.1086/339249  1
2002 Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, ... Monaco AP, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature Genetics. 30: 86-91. PMID 11743577 DOI: 10.1038/ng792  1
2001 Monaco AP, Bailey AJ. Autism. The search for susceptibility genes. Lancet. 358: S3. PMID 11784552  0.52
2001 Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, ... ... Monaco AP, et al. McLeod neuroacanthocytosis: genotype and phenotype. Annals of Neurology. 50: 755-64. PMID 11761473 DOI: 10.1002/ana.10035  0.68
2001 Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 413: 519-23. PMID 11586359 DOI: 10.1038/35097076  1
2001 Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, Monaco AP, Stein JF, Cardon LR. Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behavior Genetics. 31: 219-30. PMID 11545538 DOI: 10.1023/A:1010209629021  1
2001 Umemura A, Morita H, Li XC, Tahan S, Monaco AP, Maki T. Dissociation of hemopoietic chimerism and allograft tolerance after allogeneic bone marrow transplantation. Journal of Immunology (Baltimore, Md. : 1950). 167: 3043-8. PMID 11544287  1
2001 Rampoldi L, Dobson-Stone C, Rubio JP, Danek A, Chalmers RM, Wood NW, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Brown R, Vance J, Pericak-Vance M, Rudolf G, Carrè S, ... ... Monaco AP, et al. A conserved sorting-associated protein is mutant in chorea-acanthocytosis. Nature Genetics. 28: 119-20. PMID 11381253 DOI: 10.1038/88821  0.68
2001 Bolino A, Lonie LJ, Zimmer M, Boerkoel CF, Takashima H, Monaco AP, Lupski JR. Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy. Neurogenetics. 3: 107-9. PMID 11354824 DOI: 10.1007/s100480000101  1
2000 Maestrini E, Paul A, Monaco AP, Bailey A. Identifying autism susceptibility genes. Neuron. 28: 19-24. PMID 11086979  1
2000 Francks C, Fisher SE, Marlow AJ, Richardson AJ, Stein JF, Monaco AP. A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability. Prostaglandins, Leukotrienes, and Essential Fatty Acids. 63: 27-31. PMID 10970709 DOI: 10.1054/plef.2000.0187  1
2000 Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. American Journal of Human Genetics. 67: 357-68. PMID 10880297 DOI: 10.1086/303011  1
2000 Sudbrak R, Brown J, Dobson-Stone C, Carter S, Ramser J, White J, Healy E, Dissanayake M, Larrègue M, Perrussel M, Lehrach H, Munro CS, Strachan T, Burge S, Hovnanian A, ... Monaco AP, et al. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. Human Molecular Genetics. 9: 1131-40. PMID 10767338  1
2000 Dobson-Stone C, Cox RD, Lonie L, Southam L, Fraser M, Wise C, Bernier F, Hodgson S, Porter DE, Simpson AH, Monaco AP. Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses. European Journal of Human Genetics : Ejhg. 8: 24-32. PMID 10713884 DOI: 10.1038/sj.ejhg.5200409  1
1999 Fisher SE, Stein JF, Monaco AP. A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia). European Child & Adolescent Psychiatry. 8: 47-51. PMID 10638370  1
1999 Németh AH, Nolte D, Dunne E, Niemann S, Kostrzewa M, Peters U, Fraser E, Bochukova E, Butler R, Brown J, Cox RD, Levy ER, Ropers HH, Monaco AP, Müller U. Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3). Genomics. 60: 320-9. PMID 10493831 DOI: 10.1006/geno.1999.5929  1
1999 Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium. American Journal of Medical Genetics. 88: 492-6. PMID 10490705 DOI: 10.1002/(SICI)1096-8628(19991015)88:5<492::AID-AJMG11>3.0.CO;2-X  1
1999 Maestrini E, Korge BP, Ocaña-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Human Molecular Genetics. 8: 1237-43. PMID 10369869 DOI: 10.1093/hmg/8.7.1237  1
1999 Rubio JP, Levy ER, Dobson-Stone C, Monaco AP. Genomic organization of the human galpha14 and Galphaq genes and mutation analysis in chorea-acanthocytosis (CHAC). Genomics. 57: 84-93. PMID 10191087 DOI: 10.1006/geno.1999.5758  0.68
1999 Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, et al. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics. 21: 271-7. PMID 10080178 DOI: 10.1038/6784  0.4
1999 Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. American Journal of Human Genetics. 64: 146-56. PMID 9915953 DOI: 10.1086/302190  1
1998 Lee WL, Tay A, Ong HT, Goh LM, Monaco AP, Szepetowski P. Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family. Human Genetics. 103: 608-12. PMID 9860304 DOI: 10.1007/s004390050876  1
1998 Maestrini E, Marlow AJ, Weeks DE, Monaco AP. Molecular genetic investigations of autism. Journal of Autism and Developmental Disorders. 28: 427-37. PMID 9813778 DOI: 10.1023/A:1026056522602  1
1998 Hovnanian A, Rebouillat D, Mattei MG, Levy ER, Marié I, Monaco AP, Hovanessian AG. The human 2',5'-oligoadenylate synthetase locus is composed of three distinct genes clustered on chromosome 12q24.2 encoding the 100-, 69-, and 40-kDa forms. Genomics. 52: 267-77. PMID 9790745 DOI: 10.1006/geno.1998.5443  0.4
1998 Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U. Integrated physical and transcript map of 5q31.3-qter. European Journal of Human Genetics : Ejhg. 6: 266-74. PMID 9781031 DOI: 10.1038/sj.ejhg.5200188  1
1998 Morrissey PE, Gordon F, Shaffer D, Madras PN, Silva P, Sahyoun AI, Monaco AP, Hill T, Lewis WD, Jenkins RL. Combined liver-kidney transplantation in patients with cirrhosis and renal failure: effect of a positive cross-match and benefits of combined transplantation. Liver Transplantation and Surgery : Official Publication of the American Association For the Study of Liver Diseases and the International Liver Transplantation Society. 4: 363-9. PMID 9724473  1
1998 Woon PY, Osoegawa K, Kaisaki PJ, Zhao B, Catanese JJ, Gauguier D, Cox R, Levy ER, Lathrop GM, Monaco AP, de Jong PJ. Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library. Genomics. 50: 306-16. PMID 9676425 DOI: 10.1006/geno.1998.5319  1
1998 Monk S, Sakuntabhai A, Carter SA, Bryce SD, Cox R, Harrington L, Levy E, Ruiz-Perez VL, Katsantoni E, Kodvawala A, Munro CS, Burge S, Larrègue M, Nagy G, Rees JL, ... ... Monaco AP, et al. Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region. American Journal of Human Genetics. 62: 890-903. PMID 9529352 DOI: 10.1086/301794  0.4
1998 Greenfield A, Carrel L, Pennisi D, Philippe C, Quaderi N, Siggers P, Steiner K, Tam PP, Monaco AP, Willard HF, Koopman P. The UTX gene escapes X inactivation in mice and humans. Human Molecular Genetics. 7: 737-42. PMID 9499428 DOI: 10.1093/hmg/7.4.737  1
1998 Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. Localisation of a gene implicated in a severe speech and language disorder. Nature Genetics. 18: 168-70. PMID 9462748 DOI: 10.1038/ng0298-168  1
1997 Renault B, Hovnanian A, Bryce S, Chang JJ, Lau S, Sakuntabhai A, Monk S, Carter S, Ross CJ, Pang J, Twells R, Chamberlain S, Monaco AP, Strachan T, Kucherlapati R. A sequence-ready physical map of a region of 12q24.1. Genomics. 45: 271-8. PMID 9344649 DOI: 10.1006/geno.1997.4888  1
1997 Philippe C, Porter DE, Emerton ME, Wells DE, Simpson AH, Monaco AP. Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses. American Journal of Human Genetics. 61: 520-8. PMID 9326317  1
1997 Ishikawa-Brush Y, Powell JF, Bolton P, Miller AP, Francis F, Willard HF, Lehrach H, Monaco AP. Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. Human Molecular Genetics. 6: 1241-50. PMID 9259269 DOI: 10.1093/hmg/6.8.1241  1
1997 O'Neil JJ, Stegemann JP, Nicholson DT, Mullon CJ, Maki T, Monaco AP, Solomon BA. Immunoprotection provided by the bioartificial pancreas in a xenogeneic host. Transplantation Proceedings. 29: 2116-7. PMID 9193550 DOI: 10.1016/S0041-1345(97)00255-8  1
1996 Maki T, Monaco AP, Mullon CJ, Solomon BA. Early treatment of diabetes with porcine islets in a bioartificial pancreas. Tissue Engineering. 2: 299-306. PMID 19877961 DOI: 10.1089/ten.1996.2.299  1
1996 Maki T, O'Neil JJ, Porter J, Mullon CJ, Solomon BA, Monaco AP. Porcine islets for xenotransplantation. Transplantation. 62: 136-8. PMID 8693532 DOI: 10.1097/00007890-199607150-00028  1
1996 Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, Weeks DE, Lathrop M, Uitto J, Christiano AM. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nature Genetics. 13: 70-7. PMID 8673107 DOI: 10.1038/ng0596-70  1
1996 Maki T, O'Neill JJ, Porter J, Mullon CJ, Solomon BA, Monaco AP. Long-term function of porcine islets in xenogeneic hosts. Transplantation Proceedings. 28: 807. PMID 8623409  1
1996 Maki T, Otsu I, O'Neil JJ, Dunleavy K, Mullon CJ, Solomon BA, Monaco AP. Treatment of diabetes by xenogeneic islets without immunosuppression. Use of a vascularized bioartificial pancreas. Diabetes. 45: 342-7. PMID 8593940  1
1995 Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW. Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146. Genomics. 29: 496-502. PMID 8666400 DOI: 10.1006/geno.1995.9976  0.64
1995 Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y. High-resolution comparative mapping of the proximal region of the mouse X chromosome. Genomics. 28: 305-10. PMID 8530041 DOI: 10.1006/geno.1995.1146  0.44
1995 Maki T, Mullon CJ, Solomon BA, Monaco AP. Novel delivery of pancreatic islet cells to treat insulin-dependent diabetes mellitus. Clinical Pharmacokinetics. 28: 471-82. PMID 7656505 DOI: 10.2165/00003088-199528060-00005  1
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