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- [31] Genome-wide cell-free DNA screening: a focus on copy-number variantsGENETICS IN MEDICINE, 2021, 23 (10) : 1847 - 1853Rafalko, Jill论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USASoster, Erica论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USACaldwell, Samantha论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USAAlmasri, Eyad论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USAWestover, Thomas论文数: 0 引用数: 0 h-index: 0机构: Capital Hlth Syst, Dept Maternal Fetal Med & Perinatal Genet, Trenton, NJ USA Lab Corp Amer, La Jolla, CA 92037 USAWeinblatt, Vivian论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USACacheris, Philip论文数: 0 引用数: 0 h-index: 0机构: Lab Corp Amer, La Jolla, CA 92037 USA Lab Corp Amer, La Jolla, CA 92037 USA
- [32] THE CONTRIBUTION OF COPY NUMBER VARIANTS TO SCHIZOPHRENIA: FROM A GENOME-WIDE STUDY IN EAST ASIAN POPULATIONSEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2024, 87 : 27 - 27Chen, Yu论文数: 0 引用数: 0 h-index: 0机构: Broad Inst, Cambridge, MA USA Broad Inst, Cambridge, MA USAFeng, Qidi论文数: 0 引用数: 0 h-index: 0机构: Broad Inst, Cambridge, MA USA Broad Inst, Cambridge, MA USAYu, Mingrui论文数: 0 引用数: 0 h-index: 0机构: Broad Inst, Cambridge, MA USA Broad Inst, Cambridge, MA USALam, Max论文数: 0 引用数: 0 h-index: 0机构: IMH LKC PRECISE, Singapore, Singapore Broad Inst, Cambridge, MA USASawa, Akira论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Baltimore, MD 21218 USA Broad Inst, Cambridge, MA USATang, Jingsong论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp 2, Changsha, Hunan, Peoples R China Broad Inst, Cambridge, MA USAMa, Xiancang论文数: 0 引用数: 0 h-index: 0机构: Xi An Jiao Tong Univ, Affiliated Hosp 1, Clin Res Ctr Mental Dis Shaanxi Prov, Xian, Shaanxi, Peoples R China Broad Inst, Cambridge, MA USAChen, Wei J.论文数: 0 引用数: 0 h-index: 0机构: Natl Hlth Res Inst, Ctr Neuropsychiat Res, Zhunan Town, Peoples R China Broad Inst, Cambridge, MA USAQin, Shengying论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Bio X Inst, Shanghai, Peoples R China Broad Inst, Cambridge, MA USAYue, Weihua论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Inst Mental Hlth, Sixth Hosp, Beijing, Peoples R China Broad Inst, Cambridge, MA USAGe, Tian论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Hosp, Boston, MA 02114 USA Broad Inst, Cambridge, MA USAHuang, Hailiang论文数: 0 引用数: 0 h-index: 0机构: Broad Inst, Cambridge, MA USA Broad Inst, Cambridge, MA USA
- [33] Detection of copy number variants at new psoriasis loci identified by genome-wide association studiesBRITISH JOURNAL OF DERMATOLOGY, 2011, 165 (06) : E1 - E1Apel, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyUebe, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyEkici, A. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany论文数: 引用数: h-index:机构:Boehm, B.论文数: 0 引用数: 0 h-index: 0机构: Goethe Univ Frankfurt, Dept Internal Med 2, Div Rheumatol, Frankfurt, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyTraupe, H.论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Dept Dermatol, D-4400 Munster, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyMoessner, R.论文数: 0 引用数: 0 h-index: 0机构: Dept Dermatol, Gottingen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyBurkhardt, H.论文数: 0 引用数: 0 h-index: 0机构: Goethe Univ Frankfurt, Dept Internal Med 2, Div Rheumatol, Frankfurt, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyReis, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, GermanyHueffmeier, U.论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany Univ Erlangen Nurnberg, Inst Human Genet, D-8520 Erlangen, Germany
- [34] Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsBMC MEDICAL GENETICS, 2017, 18Uebe, Steffen论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyEhrlicher, Maria论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyEkici, Arif Buelent论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyBehrens, Frank论文数: 0 引用数: 0 h-index: 0机构: Goethe Univ, Div Rheumatol, Frankfurt, Germany Goethe Univ, IME Fraunhofer Project Grp Translat Med & Pharmac, Frankfurt, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyBoehm, Beate论文数: 0 引用数: 0 h-index: 0机构: Goethe Univ, Div Rheumatol, Frankfurt, Germany Goethe Univ, IME Fraunhofer Project Grp Translat Med & Pharmac, Frankfurt, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyHomuth, Georg论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Univ Med & Ernst Moritz Arndt, Interfac Inst Genet & Funct Genom, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanySchurmann, Claudia论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Univ Med & Ernst Moritz Arndt, Interfac Inst Genet & Funct Genom, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyVoelker, Uwe论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Univ Med & Ernst Moritz Arndt, Interfac Inst Genet & Funct Genom, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyJuenger, Michael论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Clin Dermatol, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyNauck, Matthias论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Inst Clin Chem & Lab Med, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyVoelzke, Henry论文数: 0 引用数: 0 h-index: 0机构: Ernst Moritz Arndt Univ Greifswald, Inst Community Med, Greifswald, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyTraupe, Heiko论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Dept Dermatol, Munster, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyKrawczak, Michael论文数: 0 引用数: 0 h-index: 0机构: Christian Albrechts Univ Kiel, Inst Med Informat & Stat, Kiel, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyBurkhardt, Harald论文数: 0 引用数: 0 h-index: 0机构: Goethe Univ, Div Rheumatol, Frankfurt, Germany Goethe Univ, IME Fraunhofer Project Grp Translat Med & Pharmac, Frankfurt, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyReis, Andre论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, GermanyHueffmeier, Ulrike论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Human Genet, Schwabachanlage 10, D-91054 Erlangen, Germany
- [35] Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsyMOVEMENT DISORDERS, 2019, 34 (07) : 1049 - 1059Chen, Zhongbo论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandChen, Jason A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Interdept Program Bioinformat, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandShatunov, Aleksey论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandJones, Ashley R.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandKravitz, Stephanie N.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandHuang, Alden Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Interdept Program Bioinformat, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandLawrence, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandLowe, Jennifer K.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandLewis, Cathryn M.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Social Genet & Dev Psychiat Ctr, London, England Kings Coll London, Dept Med & Mol Genet, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandPayan, Christine A. M.论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dept Pharmacol Clin, Paris, France UPMC Paris 06, Pharmacol, Univ Paris Sorbonne, Paris, France Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England论文数: 引用数: h-index:机构:Franke, Andre论文数: 0 引用数: 0 h-index: 0机构: Christian Albrechts Univ Kiel, Inst Clin Mol Biol, Kiel, Germany Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandDeloukas, Panagiotis论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, Charterhouse Sq, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandAmouyel, Philippe论文数: 0 引用数: 0 h-index: 0机构: Univ Lille, Inst Pasteur Lille, Labex Distalz,INSERM,CHU Lille, U1167,RID AGE Risk Factor & Mol Determinants Agin, Lille, France Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandTzourio, Christophe论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, Bordeaux Populat Hlth Res Ctr, CHU Bordeaux, INSERM,UMR 1219, Bordeaux, France Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandDartigues, Jean-Francois论文数: 0 引用数: 0 h-index: 0机构: Univ Bordeaux, Bordeaux Populat Hlth Res Ctr, CHU Bordeaux, INSERM,UMR 1219, Bordeaux, France Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandLudolph, Albert论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Dept Neurol, Ulm, Germany Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandBensimon, Gilbert论文数: 0 引用数: 0 h-index: 0机构: Hop La Pitie Salpetriere, AP HP, Dept Pharmacol Clin, Paris, France UPMC Paris 06, Pharmacol, Univ Paris Sorbonne, Paris, France Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandLeigh, P. Nigel论文数: 0 引用数: 0 h-index: 0机构: Univ Sussex, Trafford Ctr Biomed Res, Brighton & Sussex Med Sch, Brighton, E Sussex, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandBronstein, Jeff M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Program Movement Disorders, Dept Neurol, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandCoppola, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Interdept Program Bioinformat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst, Ctr Neurobehav Genet, Los Angeles, CA 90095 USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandGeschwind, Daniel H.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA Kings Coll London, Social Genet & Dev Psychiat Ctr, London, England Kings Coll London, Dept Med & Mol Genet, London, England Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, EnglandAl-Chalabi, Ammar论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England
- [36] Genome-wide Scan of Genetic Variants Associated with DNA Copy Number Aberrations in Lung CancerGENETIC EPIDEMIOLOGY, 2009, 33 (08) : 792 - 793Zhang, Qunyuan论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO 63130 USA Washington Univ, Sch Med, St Louis, MO 63130 USADing, Li论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO 63130 USA Washington Univ, Sch Med, St Louis, MO 63130 USALin, Ling论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO 63130 USA Washington Univ, Sch Med, St Louis, MO 63130 USABorecki, Ingrid论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO 63130 USA Washington Univ, Sch Med, St Louis, MO 63130 USAProvince, Michael A.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO 63130 USA Washington Univ, Sch Med, St Louis, MO 63130 USA
- [37] Genome-wide analysis identifies a role for common copy number variants in specific language impairmentEuropean Journal of Human Genetics, 2015, 23 : 1370 - 1377Nuala H Simpson论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryFabiola Ceroni论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryRose H Reader论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryLaura E Covill论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryJulian C Knight论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryElizabeth R Hennessy论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryPatrick F Bolton论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryGina Conti-Ramsden论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryAnne O'Hare论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryGillian Baird论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatrySimon E Fisher论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent PsychiatryDianne F Newbury论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Centre for Human Genetics,Departments of Child and Adolescent Psychiatry
- [38] Genome-wide analysis identifies a role for common copy number variants in specific language impairmentEUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (10) : 1370 - 1377Simpson, Nuala H.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandCeroni, Fabiola论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandReader, Rose H.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandCovill, Laura E.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandKnight, Julian C.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandHennessy, Elizabeth R.论文数: 0 引用数: 0 h-index: 0机构: Univ Aberdeen, Univ Child Hlth & DMDE, Aberdeen, Scotland Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandBolton, Patrick F.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, Dept Child Psychiat, London WC2R 2LS, England Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Ctr, Dept & Adolescent Psychiat, London WC2R 2LS, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandConti-Ramsden, Gina论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Psychol Sci, Manchester, Lancs, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandO'Hare, Anne论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, Dept Reprod & Dev Sci, Edinburgh, Midlothian, Scotland Evelina Childrens Hosp, Childrens Neurosci Dept, London, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandBaird, Gillian论文数: 0 引用数: 0 h-index: 0机构: Kings Hlth Partners, London, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandFisher, Simon E.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Psycholinguist, Nijmegen, Netherlands Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, NL-6525 ED Nijmegen, Netherlands Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, EnglandNewbury, Dianne F.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford St Johns Coll, Oxford OX1 3JP, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
- [39] Genome-Wide Copy Number Variation Analysis Identifies Deletion Variants Associated With Ankylosing SpondylitisARTHRITIS & RHEUMATOLOGY, 2014, 66 (08) : 2103 - 2112Jung, Seung-Hyun论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Catholic Univ Korea, Seoul, South KoreaYim, Seon-Hee论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Catholic Univ Korea, Seoul, South KoreaHu, Hae-Jin论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Catholic Univ Korea, Seoul, South Korea论文数: 引用数: h-index:机构:Lee, Joo-Hyun论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Inje Univ, Ilsan Paik Hosp, Goyang, South Korea Catholic Univ Korea, Seoul, South KoreaSheen, Dong-Hyuk论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ Hosp, Taejon, South Korea Catholic Univ Korea, Seoul, South KoreaLim, Mi-Kyoung论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ Hosp, Taejon, South Korea Catholic Univ Korea, Seoul, South KoreaKim, Soon-Young论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South KoreaPark, Sung-Won论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Catholic Univ Korea, Seoul, South KoreaKim, So-Hee论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Korea, Seoul, South Korea Catholic Univ Korea, Seoul, South Korea论文数: 引用数: h-index:机构:Kim, Tae-Hwan论文数: 0 引用数: 0 h-index: 0机构: Hanyang Univ, Hosp Rheumat Dis, Seoul 133792, South Korea Catholic Univ Korea, Seoul, South KoreaShim, Seung-Cheol论文数: 0 引用数: 0 h-index: 0机构: Chungnam Natl Univ Hosp, Taejon, South Korea Catholic Univ Korea, Seoul, South Korea论文数: 引用数: h-index:机构:
- [40] Genome-wide copy number variation analysis of hepatitis B infection in a Japanese populationHuman Genome Variation, 8Masataka Kikuchi论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineKaori Kobayashi论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineNao Nishida论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineHiromi Sawai论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineMasaya Sugiyama论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineMasashi Mizokami论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineKatsushi Tokunaga论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of MedicineAkihiro Nakaya论文数: 0 引用数: 0 h-index: 0机构: Osaka University,Department of Genome Informatics, Graduate School of Medicine