부산대학교 도서관

Ibrahim, Abdulla; Barnes, Daniel R; Dunlop, Jacqueline; Barrowdale, Daniel; Antoniou, Antonis C; Berg, Jonathan N

European Journal of Human Genetics. Nov2014, Vol. 22 Issue 11, p1330-1333. 4p.

Martin, Amy J.; Grant, Andrew; Ashfield, Alison M.; Palmer, Colin N.; Baker, Lee; Quinlan, Philip R.; Purdie, Colin A.; Thompson, Alastair M.; Jordan, Lee B.; Berg, Jonathan N

BMC Research Notes. 2011, Vol. 4 Issue 1, p72-78. 7p.

Spinelli, Laura; Black, Fiona M; Berg, Jonathan N; Eickholt, Britta J; Leslie, Nicholas R

Journal of Medical Genetics. Feb 01, 2015 52(2):128-134

Weinsheimer, Shantel; Bendjilali, Nasrine; Nelson, Jeffrey; Guo, Diana E; Zaroff, Jonathan G; Sidney, Stephen; Mcculloch, Charles E; Al Shahi Salman, Rustam; Berg, Jonathan N; Koeleman, Bobby P. C; Simon, Matthias; Bostroem, Azize; Fontanella, Marco; Sturiale, Carmelo Lucio; Pola, Roberto; Puca, Alfredo; Lawton, Michael T; Young, William L; Pawlikowska, Ludmila; Klijn, Catharina J. M; Kim, Helen

Journal of Neurology, Neurosurgery, and Psychiatry, 87, 9, pp. 916-23
Weinsheimer, S, Bendjilali, N, Nelson, J, Guo, D E, Zaroff, J G, Sidney, S, McCulloch, C E, Al-Shahi Salman, R, Berg, J N, Koeleman, B P C, Simon, M, Bostroem, A, Fontanella, M, Sturiale, C L, Pola, R, Puca, A, Lawton, M T, Young, W L, Pawlikowska, L, Klijn, C J M, Kim, H 2016, ' Genome-wide association study of sporadic brain arteriovenous malformations ', Journal of Neurology, Neurosurgery & Psychiatry . https://doi.org/10.1136/jnnp-2015-312272
Journal of Neurology Neurosurgery & Psychiatry, vol 87, iss 9

BERG, JONATHAN N; QUABA, A A; GEORGANTOPOULOU, A; PORTEOUS, MARY E M

Journal of Medical Genetics. Aug 01, 2000 37(8):e12-e12

Michael Yates T; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.; Ng OH; Ninewells Hospital and Medical School, University of Dundee, Dundee, United Kingdom.; Offiah AC; Academic Unit of Child Health, University of Sheffield, Sheffield, United Kingdom.; Radiology Department, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.; Willoughby J; Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.; Berg JN; Dundee Clinical Genetics Service, Ninewells Hospital and Medical School, Dundee, United Kingdom.; Johnson DS; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, United Kingdom.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Eggens, Veerle RC; Barth, Peter G; Niermeijer, Jikke-Mien F; Berg, Jonathan N; Darin, Niklas; Dixit, Abhijit; Fluss, Joel; Foulds, Nicola; Fowler, Darren; Hortobágyi, Tibor; Jacques, Thomas; King, Mary D; Makrythanasis, Periklis; Mátñ, Adrienn; Nicoll, James AR; O'Rourke, Declan; Price, Sue; Williams, Andrew N; Wilson, Louise; Suri, Mohnish; Sztriha, Laszlo; Dijns-de Wissel, Marit B; van Meegen, Mia T; van Ruissen, Fred; Aronica, Eleonora; Troost, Dirk; Majoie, Charles BLM; Marquering, Henk A; Poll-Thñ, Bwee Tien; Baas, Frank

Orphanet Journal of Rare Diseases. February 13, 2014, Vol. 9

McLeish L; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.; Reis MM; Stewart C; Goudie DR; Berg JN; Harvie M; Hanning KA; Vysny H; Steel CM

Publisher: Informa Healthcare Country of Publication: England NLM ID: 9421097 Publication Model: Print Cited Medium: Internet ISSN: 1532-7558 (Electronic) Linking ISSN: 10705503 NLM ISO Abbreviation: Int J Behav Med Subsets: MEDLINE

Nabais Sá MJ; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Jensik PJ; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL, USA.; McGee SR; Department of Physiology, Southern Illinois University School of Medicine, Carbondale, IL, USA.; Parker MJ; Sheffield Clinical Genetics Service, OPD2 Northern General Hospital, Sheffield, UK.; Lahiri N; Department of Clinical Genetics, St George's University Hospitals NHS Foundation Trust & St George's, University of London, London, UK.; McNeil EP; Dartmouth Geisel School of Medicine, Hanover, NH, USA.; Kroes HY; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Hagerman RJ; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis School of Medicine, Sacramento, Sacramento, CA, USA.; Department of Pediatrics, University of California Davis Medical Center, Sacramento, Sacramento, CA, USA.; Harrison RE; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Montgomery T; Northern Genetics Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Splitt M; Northern Genetics Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Palmer EE; Sydney Children's Hospital, Randwick, NSW, Australia.; School of Women's and Children's Health, UNSW Medicine, The University of New South Wales, Sydney, NSW, Australia.; Sachdev RK; Sydney Children's Hospital, Randwick, NSW, Australia.; School of Women's and Children's Health, UNSW Medicine, The University of New South Wales, Sydney, NSW, Australia.; Mefford HC; Department of Pediatrics, Division of Genetic Medicine, University of Washington-Seattle, Seattle, WA, USA.; Scott AA; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, WA, USA.; Martinez-Agosto JA; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Lorenz R; Ludwig-Konrad-Str. 14, Bad Wildungen, Germany.; Orenstein N; Pediatric Genetics Clinic, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.; Berg JN; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, Angus, UK.; Clinical Genetics, University of Dundee, Dundee, Angus, UK.; Amiel J; Département de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique, INSERM UMR 1163, Institut Imagine, Paris, France.; Heron D; Département de Génétique, Hôpital Pitié-Salpêtrière, Assistance publique-Hôpitaux de Paris, Paris, France.; Keren B; Département de Génétique, Hôpital Pitié-Salpêtrière, Assistance publique-Hôpitaux de Paris, Paris, France.; Cobben JM; Department of Pediatrics, Amsterdam University Medical Centers, Amsterdam, The Netherlands.; North West Thames Genetics NHS, Northwick Park Hospital, London, UK.; Menke LA; Department of Pediatrics, Amsterdam University Medical Centers, Amsterdam, The Netherlands.; Marco EJ; Department of Child Neurology, Cortica Healthcare, San Rafael, CA, USA.; Graham JM Jr; Division of Clinical Genetics and Dysmorphology, Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA, USA.; Pierson TM; Department of Pediatrics, Department of Neurology, and the Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.; Karimiani EG; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, London, UK.; Maroofian R; Genetics Research Centre, Molecular and Clinical Sciences Institute, St George's, University of London, London, UK.; Manzini MC; GW Institute for Neuroscience, Department of Pharmacology and Physiology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.; Cauley ES; GW Institute for Neuroscience, Department of Pharmacology and Physiology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.; Colombo R; Faculty of Medicine'Agostino Gemelli'Catholic University of the Sacred Heart, Rome, Italy.; Center for the Study of Rare Inherited Diseases (CeSMER), Niguarda Ca' Granda Metropolitan Hospital, Milan, Italy.; Odent S; Service de Génétique Clinique, CLAD-Ouest CHU Rennes, Univ Rennes, CNRS 6290 Institut de Génétique et Développement de Rennes (IGDR), Rennes, France.; Dubourg C; Univ Rennes, CHU Rennes, CNRS, IGDR, UMR 6290, Rennes, France.; Phornphutkul C; Division of Human Genetics, Department of Pediatrics, Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Providence, RI, USA.; de Brouwer APM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; de Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. Bert.deVries@radboudumc.nl.; Vulto-vanSilfhout AT; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Maniam P; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.; Zhou K; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.; Lonergan M; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.; Berg JN; Clinical Genetics, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.; Goudie DR; Clinical Genetics, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.; Newey PJ; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, Scotland.

Publisher: Endocrine Society Country of Publication: United States NLM ID: 101697997 Publication Model: eCollection Cited Medium: Internet ISSN: 2472-1972 (Electronic) Linking ISSN: 24721972 NLM ISO Abbreviation: J Endocr Soc Subsets: PubMed not MEDLINE

Littlejohn LA; Clinical Genetics, University of Dundee, Dundee, Angus, UK. lucy_littlejohn@outlook.com.; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, Angus, UK. lucy_littlejohn@outlook.com.; Gibbs J; Department of Pathology, Ninewells Hospital and Medical School, Dundee, Angus, UK.; Jordan LB; Department of Pathology, Ninewells Hospital and Medical School, Dundee, Angus, UK.; Miedzybrodzka ZH; Department of Clinical Genetics, Ashgrove House, Aberdeen, UK.; Bell C; Department of Clinical Genetics, Ashgrove House, Aberdeen, UK.; Goudie D; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, Angus, UK.; Dunlop J; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, Angus, UK.; Berg JN; Clinical Genetics, University of Dundee, Dundee, Angus, UK.; Department of Clinical Genetics, Ninewells Hospital and Medical School, Dundee, Angus, UK.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Newey PJ; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY, Scotland, United Kingdom.; Berg JN; Clinical Genetics, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY Scotland, United Kingdom.; Zhou K; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY, Scotland, United Kingdom.; Palmer CNA; Division of Molecular & Clinical Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY, Scotland, United Kingdom.; Thakker RV; Academic Endocrine Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, OX3 7LJ United Kingdom.

Publisher: Endocrine Society Country of Publication: United States NLM ID: 101697997 Publication Model: eCollection Cited Medium: Internet ISSN: 2472-1972 (Electronic) Linking ISSN: 24721972 NLM ISO Abbreviation: J Endocr Soc Subsets: PubMed not MEDLINE

Clark GR; Department of Medical Genetics (G.R.C., E.R.M.), University of Cambridge and National Institute for Health Research, Cambridge Biomedical Research Centre, Cambridge CB2 0QQ, United Kingdom; Medical Research Council (MRC) Cancer Unit (M.S., E.G., C.F.), University of Cambridge, Hutchison/MRC Research Centre, Cambridge CB2 0XZ, United Kingdom; Centre for Rare Diseases and Personalized Medicine (D.M.W., G.K., E.R.W.), University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom; West Midlands Regional Genetics Service (G.K., E.R.W.), Birmingham Women's Hospital, Birmingham B15 2TG, United Kingdom; Division of Genetics and Molecular Medicine (M.A.S., R.C.T.), King's College London School of Medicine, Guy's Hospital, London WC2R 2LS, United Kingdom; Department of Clinical Genetics (J.N.B.), University of Dundee, Ninewells Hospital and Medical School, Dundee DD1 9SY, United Kingdom; Department of Clinical Genetics (E.K.), Royal Hospital for Sick Children (Yorkhill), Glasgow G3 8SJ, United Kingdom; and Department of Medical Genetics (P.J.M.), Queen's University Belfast, Belfast Health and Social Care Trust, Belfast BT9 7AB, United Kingdom.; Sciacovelli M; Gaude E; Walsh DM; Kirby G; Simpson MA; Trembath RC; Berg JN; Woodward ER; Kinning E; Morrison PJ; Frezza C; Maher ER

Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1945-7197 (Electronic) Linking ISSN: 0021972X NLM ISO Abbreviation: J Clin Endocrinol Metab Subsets: MEDLINE

Hall CEJ; Human Genetics, Centre For Oncology and Molecular Medicine, University of Dundee, DD1 9SY, UK.; Cunningham JJP; Hislop RG; Berg JN

Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE

Lux A; University Hospital Mannheim and Institute of Molecular Biology and Cell Culture Technology, University of Applied Sciences Mannheim, 68163 Mannheim, Germany. a.lux@fh-mannheim.de; Beil C; Majety M; Barron S; Gallione CJ; Kuhn HM; Berg JN; Kioschis P; Marchuk DA; Hafner M

Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print-Electronic Cited Medium: Print ISSN: 0021-9258 (Print) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE