المؤلفون: Zewei Xiong, Thuan-Quoc Thach, Yan Dora Zhang, Pak Chung Sham

المصدر: HGG Advances, Vol 5, Iss 2, Pp 100272- (2024)

مصطلحات موضوعية: generalized LD score regression, partition heritability, functional enrichment, GWAS summary statistics, complex human traits, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666247724000113; https://doaj.org/toc/2666-2477

URL الوصول: https://doaj.org/article/efba3bafc11443e5810d5aca86b8ad11

المؤلفون: Nadav Brandes, Omer Weissbrod, Michal Linial

المصدر: Genome Biology, Vol 23, Iss 1, Pp 1-32 (2022)

مصطلحات موضوعية: Statistical genetics, Human phenotypes, Complex human traits, GWAS, Genome-wide association studies, PRS, Biology (General), QH301-705.5, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1474-760X

URL الوصول: https://doaj.org/article/f34c94b0917f46d98f6c1a03acf39d02

المؤلفون: Zhu, Jun, Chen, Congying, Yang, Bin, Guo, Yuanmei, Ai, Huashui, Ren, Jun, Peng, Zhiyu, Tu, Zhidong, Yang, Xia, Meng, Qingying, Friend, Stephen, Huang, Lusheng

المصدر: BMC Genomics. 16(1)

مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Pediatric Research Initiative, Aetiology, 2.1 Biological and endogenous factors, Generic health relevance, Anemia, Animals, Body Height, Chromosome Mapping, Genome, Human, Genome-Wide Association Study, Genotype, Humans, Liver, Mice, Phenotype, Quantitative Trait Loci, Swine, Transforming Growth Factor beta3, ras GTPase-Activating Proteins, Systems genetics, Swine model, Complex human traits, Information and Computing Sciences, Medical and Health Sciences, Bioinformatics, Biological sciences, Biomedical and clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/67x9j6fd

المؤلفون: Parker, Katherine, Erzurumluoglu, A Mesut, Rodriguez, Santiago

مصطلحات موضوعية: Y chromosome, Y haplogroups, complex human traits, complex locus, genetic association analyses, genetic epidemiology, Chromosomes, Human, Genetic Association Studies, Genetic Variation, Genetics, Population, Genome-Wide Association Study, Haplotypes, Humans, Male, Models, Genetic, Molecular Epidemiology, Multifactorial Inheritance, Quantitative Trait Loci, Recombination, Sex Determination Processes

وصف الملف: application/pdf; application/zip; text/xml

Relation: https://www.repository.cam.ac.uk/handle/1810/312286

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/312286
https://doi.org/10.17863/CAM.59379

المؤلفون: Katherine Parker, A. Mesut Erzurumluoglu, Santiago Rodriguez

المصدر: Genes; Volume 11; Issue 11; Pages: 1273

مصطلحات موضوعية: Y chromosome, Y haplogroups, complex locus, genetic association analyses, genetic epidemiology, complex human traits

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Human Genomics and Genetic Diseases; https://dx.doi.org/10.3390/genes11111273

الاتاحة: https://doi.org/10.3390/genes11111273

المؤلفون: Psychiat Genomics Consortium, Lönnqvist, Jouko, Paunio, Tiina

المساهمون: Clinicum, Department of Psychiatry, HUS Psychiatry

مصطلحات موضوعية: COMPLEX HUMAN TRAITS, BODY-MASS INDEX, WIDE ASSOCIATION, PARTITIONING HERITABILITY, SUSCEPTIBILITY LOCI, SNP HERITABILITY, HUMAN HEIGHT, SCHIZOPHRENIA, INFORMATION, STATISTICS, Biomedicine, Neurology and psychiatry

وصف الملف: application/pdf

Relation: This research is supported by the Australian National Health and Medical Research Council (1080157, 1087889) and the Australian Research Council (DP160102126, FT160100229). This research has been conducted using the UK Biobank Resource. UK Biobank Research Ethics Committee (REC) approval number is 11/NW/0382. Our reference number approved by UK Biobank is 14575. GERA data came from a grant, the Resource for Genetic Epidemiology Research in Adult Health and Aging (RC2 AG033067; Schaefer and Risch, PIs) awarded to the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) and the UCSF Institute for Human Genetics. The RPGEH was supported by grants from the Robert Wood Johnson Foundation, the Wayne and Gladys Valley Foundation, the Ellison Medical Foundation, Kaiser Permanente Northern California, and the Kaiser Permanente National and Northern California Community Benefit Programs. The RPGEH and the Resource for Genetic Epidemiology Research in Adult Health and Aging are described in the GERA website (see Web Resources). This study makes use of data generated by the Wellcome Trust Case-Control Consortium. A full list of the investigators who contributed to the generation of the WTCCC data is available online. Funding for the WTCCC project was provided by the Wellcome Trust under awards 076113, 085475, and 090355.; Psychiat Genomics Consortium , Lönnqvist , J & Paunio , T 2018 , ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ' , American Journal of Human Genetics , vol. 102 , no. 6 , pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021; http://hdl.handle.net/10138/305741; 254082cb-f767-4dfd-a219-0cfeb172a567; 85046126170; 000434946200014

الاتاحة: http://hdl.handle.net/10138/305741

المؤلفون: Ip, Hill F., Jansen, Rick, Abdellaoui, Abdel, Bartels, Meike, Boomsma, Dorret I., Nivard, Michel G.

المصدر: Ip , H F , Jansen , R , Abdellaoui , A , Bartels , M , Boomsma , D I , Nivard , M G & UK Brain Expression Consortium 2018 , ' Characterizing the Relation Between Expression QTLs and Complex Traits : Exploring the Role of Tissue Specificity ' , Behavior Genetics , vol. 48 , no. 5 , pp. 374-385 . https://doi.org/10.1007/s10519-018-9914-2

مصطلحات موضوعية: Brain, Complex human traits, Enrichment, eQTL discovery, Gene expression, Genome-wide, SLDSR, Stratified linkage disequilibrium score regression, Tissue-specificity, Whole blood, /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_, name=Netherlands Twin Register (NTR)

الاتاحة: https://research.vu.nl/en/publications/030b64a0-05a4-4344-b7f0-1609763d6d16
https://doi.org/10.1007/s10519-018-9914-2
https://hdl.handle.net/1871.1/030b64a0-05a4-4344-b7f0-1609763d6d16
http://www.scopus.com/inward/record.url?scp=85050367360&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85050367360&partnerID=8YFLogxK

المؤلفون: Ip, HF, Jansen, R, Abdellaoui, A, Bartels, M, UK Brain Expression Consortium, ., Boomsma, DI, Nivard, MG

المصدر: Behavior Genetics , 48 (5) pp. 374-385. (2018)

مصطلحات موضوعية: Brain, Complex human traits, Enrichment, Gene expression, Genome-wide, SLDSR, Stratified linkage disequilibrium score regression, Tissue-specificity, Whole blood, eQTL discovery

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10055150/1/10.1007_s10519-018-9914-2.pdf; https://discovery.ucl.ac.uk/id/eprint/10055150/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10055150/1/10.1007_s10519-018-9914-2.pdf
https://discovery.ucl.ac.uk/id/eprint/10055150/

المؤلفون: David J. Cutler, Min A. Jhun, Michael P. Epstein, Jacob L. Moore, Richard Duncan, Patricia A. Peyser, Lawrence F. Bielak, Wei Zhao, Debashis Ghosh, K. Alaine Broadaway, Sharon L.R. Kardia, Erin B. Ware, Jennifer A. Smith

المصدر: The American Journal of Human Genetics. 98(3):525-540

مصطلحات موضوعية: 0301 basic medicine, Multivariate statistics, Multivariate analysis, Genotype, Blood Pressure, Computational biology, Biology, Cardiovascular System, 01 natural sciences, Article, Body Mass Index, 010104 statistics & probability, 03 medical and health sciences, Similarity (network science), Pleiotropy, Databases, Genetic, Covariate, pleiotropy, Genetics, Humans, Exome, Genetics(clinical), 0101 mathematics, rare variant, Genetic Association Studies, Genetics (clinical), Oligonucleotide Array Sequence Analysis, Models, Genetic, Genome, Human, Cholesterol, HDL, Univariate, Nonparametric statistics, Genetic Variation, gene mapping, Phenotype, 030104 developmental biology, Genetic epidemiology, complex human traits, Multivariate Analysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::640b0b8ec5f9030d83e89fd18cbf3d45

المؤلفون: Rudra, Pratyaydipta, Broadaway, K. Alaine, Ware, Erin B., Jhun, Min A., Bielak, Lawrence F., Zhao, Wei, Smith, Jennifer A., Peyser, Patricia A., Kardia, Sharon L.R., Epstein, Michael P., Ghosh, Debashis

مصطلحات موضوعية: pleiotropy, longitudinal data, complex human traits, gene mapping, rare variant, Biological Chemistry, Genetics, Molecular, Cellular and Developmental Biology, Health Sciences, Science

وصف الملف: application/pdf

Relation: Rudra, Pratyaydipta; Broadaway, K. Alaine; Ware, Erin B.; Jhun, Min A.; Bielak, Lawrence F.; Zhao, Wei; Smith, Jennifer A.; Peyser, Patricia A.; Kardia, Sharon L.R.; Epstein, Michael P.; Ghosh, Debashis (2018). "Testing cross‐phenotype effects of rare variants in longitudinal studies of complex traits." Genetic Epidemiology 42(4): 320-332.; https://hdl.handle.net/2027.42/144294; Genetic Epidemiology; Sun, J., Oualkacha, K., Forgetta, V., Zheng, H. F., Richards, J. B., Ciampi, A., & Greenwood, C. M. ( 2016 ). A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects. European Journal of Human Genetics, 24 ( 9 ), 1344 – 1351.; Galesloot, T. E., Van Steen, K., Kiemeney, L. A., Janss, L. L., & Vermeulen, S. H. ( 2014 ). A comparison of multivariate genome‐wide association methods. PloS One, 9 ( 4 ), e95923.; Gottesman, R. F., Schneider, A. 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الاتاحة: https://hdl.handle.net/2027.42/144294
https://doi.org/10.1002/gepi.22121

المؤلفون: Psychiat Genomics Consortium, Lönnqvist, Jouko, Paunio, Tiina

المساهمون: Clinicum, Department of Psychiatry, HUS Psychiatry

مصطلحات موضوعية: COMPLEX HUMAN TRAITS, BODY-MASS INDEX, WIDE ASSOCIATION, PARTITIONING HERITABILITY, SUSCEPTIBILITY LOCI, SNP HERITABILITY, HUMAN HEIGHT, SCHIZOPHRENIA, INFORMATION, STATISTICS, 3111 Biomedicine, 3124 Neurology and psychiatry

Relation: http://hdl.handle.net/10138/305741

الاتاحة: http://hdl.handle.net/10138/305741

المؤلفون: Guiyan Ni, Gerhard Moser, Naomi R. Wray, S. Hong Lee, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James T.R. Walters, Kai-How Farh, Peter A. Holmans, Phil Lee, Brendan Bulik-Sullivan, David A. Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu A. Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C.K. Chan, Ronald Y.L. Chen, Eric Y.H. Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del Favero, Ditte Demontis, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan Eriksson, Valentina Escott-Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti-Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Vera Golimbet, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Mads V. Hollegaard, David M. Hougaard, Masashi Ikeda, Inge Joa, Antonio Juliá, René S. Kahn, Luba Kalaydjieva, Sena Karachanak-Yankova, Juha Karjalainen, David Kavanagh, Matthew C. Keller, James L. Kennedy, Andrey Khrunin, Yunjung Kim, Janis Klovins, James A. Knowles, Bettina Konte, Vaidutis Kucinskas, Zita Ausrele Kucinskiene, Hana Kuzelova-Ptackova, Anna K. Kähler, Claudine Laurent, Jimmy Lee Chee Keong, Sophie E. Legge, Bernard Lerer, Miaoxin Li, Tao Li, Kung-Yee Liang, Jeffrey Lieberman, Svetlana Limborska, Carmel M. Loughland, Jan Lubinski, Jouko Lönnqvist, Milan Macek, Patrik K.E. Magnusson, Brion S. Maher, Wolfgang Maier, Jacques Mallet, Sara Marsal, Manuel Mattheisen, Morten Mattingsda, Robert W. McCarley, Colm McDonald, Andrew M. McIntosh, Sandra Meier, Carin J. Meijer, Bela Melegh, Ingrid Melle, Raquelle I. Mesholam-Gately, Andres Metspalu, Patricia T. Michie, Lili Milani, Vihra Milanova, Younes Mokrab, Derek W. Morris, Ole Mors, Kieran C. Murphy, Robin M. Murray, Inez Myin-Germeys, Bertram Müller-Myhsok, Mari Nelis, Igor Nenadic, Deborah A. Nertney, Gerald Nestadt, Kristin K. Nicodemus, Liene Nikitina-Zake, Laura Nisenbaum, Annelie Nordin, Eadbhard O’Callaghan, Colm O’Dushlaine, F. Anthony O’Neill, Sang-Yun Oh, Ann Olinc, Line Olsen, Jim Van Os, Christos Pantelis, George N. Papadimitriou, Sergi Papio, Elena Parkhomenko, Michele T. Pato, Tiina Paunio, Milica Pejovic-Milovancevic, Diana O. Perkins, Olli Pietiläinenl, Jonathan Pimm, Andrew J. Pocklington, John Powell, Alkes Price, Ann E. Pulver, Shaun M. Purcell, Digby Quested, Henrik B. Rasmussen, Abraham Reichenberg, Mark A. Reimers, Alexander L. Richards, Joshua L. Roffman, Panos Roussos, Douglas M. Ruderfer, Veikko Salomaa, Alan R. Sanders, Ulrich Schall, Christian R. Schubert, Thomas G. Schulze, Sibylle G. Schwab, Edward M. Scolnick, Rodney J. Scott, Larry J. Seidman, Jianxin Shi, Engilbert Sigurdsson, Teimuraz Silagadze, Jeremy M. Silverman, Kang Sim, Petr Slominsky, Jordan W. Smoller, Hon-Cheong So, Chris C.A. Spencer, Eli A. Stah, Hreinn Stefansson, Stacy Steinberg, Elisabeth Stogmann, Richard E. Straub, Eric Strengman, Jana Strohmaier, T. Scott Stroup, Mythily Subramaniam, Jaana Suvisaari, Dragan M. Svrakic, Jin P. Szatkiewicz, Erik Söderman, Srinivas Thirumalai, Draga Toncheva, Sarah Tosato, Juha Veijola, John Waddington, Dermot Walsh, Dai Wang, Qiang Wang, Bradley T. Webb, Mark Weiser, Dieter B. Wildenauer, Nigel M. Williams, Stephanie Williams, Stephanie H. Witt, Aaron R. Wolen, Emily H.M. Wong, Brandon K. Wormley, Hualin Simon Xi, Clement C. Zai, Xuebin Zheng, Fritz Zimprich, Kari Stefansson, Peter M. Visscher, Rolf Adolfsson, Ole A. Andreassen, Douglas H.R. Blackwood, Elvira Bramon, Joseph D. Buxbaum, Anders D. Børglum, Sven Cichon, Ariel Darvasi, Enrico Domenici, Hannelore Ehrenreich, Tõnu Esko, Pablo V. Gejman, Michael Gill, Hugh Gurling, Christina M. Hultman, Nakao Iwata, Assen V. Jablensky, Erik G. Jönsson, Kenneth S. Kendler, George Kirov, Jo Knight, Todd Lencz, Douglas F. Levinson, Qingqin S. Li, Jianjun Liu, Anil K. Malhotra, Steven A. McCarrol, Andrew McQuillin, Jennifer L. Moran, Preben B. Mortensen, Bryan J. Mowry, Markus M. Nöthen, Roel A. Ophoff, Michael J. Owen, Aarno Palotie, Carlos N. Pato, Tracey L. Petryshen, Danielle Posthuma, Marcella Rietsche, Brien P. Riley, Dan Rujescu, Pak C. Sham, Pamela Sklar, David St Clair, Daniel R. Weinberger, Jens R. Wendland, Thomas Werge, Mark J. Daly, Patrick F. Sullivan, Michael C. O’Donovan

المساهمون: APH - Mental Health, ANS - Complex Trait Genetics, Adult Psychiatry, Ni, Guiyan, Moser, Gerhard, Wray, Naomi R, Lee, S Hong, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Amsterdam Neuroscience - Complex Trait Genetics, Complex Trait Genetics, Clinicum, Department of Psychiatry, HUS Psychiatry

المصدر: American journal of human genetics, 102(6), 1185-1194. Cell Press
The American Journal of Human Genetics
Agerbo, E & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018, ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ', American Journal of Human Genetics, vol. 102, no. 6, pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021
Posthuma, D & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018, ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ', American Journal of Human Genetics, vol. 102, no. 6, pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021
American Journal of Human Genetics, 102(6), 1185-1194. Cell Press
American Journal of Human Genetics, 102(6), 1185. Cell Press
American journal of human genetics, vol 102, iss 6
American journal of human genetics
The American journal of human genetics 102(6), 1185-1194 (2018). doi:10.1016/j.ajhg.2018.03.021

مصطلحات موضوعية: 0301 basic medicine, Linkage disequilibrium, Schizophrenia/genetics, INFORMATION, Restricted maximum likelihood, Inheritance Patterns, linkage disequilibrium score regression, Bioinformatics, Medical and Health Sciences, 3124 Neurology and psychiatry, Linkage Disequilibrium, biasedness, 0302 clinical medicine, Statistics, Databases, Genetic, WIDE ASSOCIATION, Genetics(clinical), PARTITIONING HERITABILITY, Genetics (clinical), Genetics & Heredity, education.field_of_study, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Likelihood Functions, Genome, Body Height/genetics, accuracy, Regression analysis, Single Nucleotide, Biological Sciences, Polymorphism, Single Nucleotide/genetics, genetic correlation, Regression, STATISTICS, genomic restricted maximum likelihood, Mental Health, Phenotype, Regression Analysis, COMPLEX HUMAN TRAITS, Single Nucleotide/genetics, Human, Adult, SUSCEPTIBILITY LOCI, Genotype, SNP heritability, body mass index, genome-wide SNPs, height, schizophrenia, Population, Haplotypes/genetics, Biology, Genetic correlation, Polymorphism, Single Nucleotide, 03 medical and health sciences, Databases, Genetic, ddc:570, Report, Genetics, Humans, Linkage Disequilibrium/genetics, Computer Simulation, Polymorphism, education, linkage disequilibrium score regression (LDSC), Genome, Human, Human Genome, genetic architecture, Genetic architecture, Body Height, Brain Disorders, Inheritance Patterns/genetics, BODY-MASS INDEX, 030104 developmental biology, Haplotypes, Sample size determination, Schizophrenia, 3111 Biomedicine, HUMAN HEIGHT, 030217 neurology & neurosurgery

وصف الملف: application/pdf; image/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7da58790da12a5d173c787aa331767e
https://pubmed.ncbi.nlm.nih.gov/29754766

المؤلفون: Congying Chen, Zhidong Tu, Lusheng Huang, Huashui Ai, Yuanmei Guo, Xia Yang, Stephen H. Friend, Zhiyu Peng, Jun Ren, Jun Zhu, Bin Yang, Qingying Meng

المصدر: Zhu, J; Chen, C; Yang, B; Guo, Y; Ai, H; Ren, J; et al.(2015). A systems genetics study of swine illustrates mechanisms underlying human phenotypic traits. BMC Genomics, 16(1). doi: 10.1186/s12864-015-1240-y. UCLA: Retrieved from: http://www.escholarship.org/uc/item/67x9j6fd
BMC genomics, vol 16, iss 1
BMC Genomics

مصطلحات موضوعية: Pediatric Research Initiative, Genotype, Swine, Bioinformatics, Quantitative Trait Loci, Genome-wide association study, Biology, Swine model, Medical and Health Sciences, Mice, Transforming Growth Factor beta3, Information and Computing Sciences, Genetics, SNP, Animals, Humans, 2.1 Biological and endogenous factors, Human height, Aetiology, Complex human traits, Gene, Systems genetics, Genetic association, 2. Zero hunger, Genome, Genome, Human, Human Genome, Chromosome Mapping, Anemia, Phenotypic trait, Biological Sciences, Phenotype, Genetic architecture, Body Height, Liver, ras GTPase-Activating Proteins, Generic health relevance, Research Article, Biotechnology, Human, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413728d135632ee28e45ef142249b689
http://www.escholarship.org/uc/item/67x9j6fd

المؤلفون: Ozturk, Ali

المصدر: Yale Medicine Thesis Digital Library

مصطلحات موضوعية: complex human traits, genetic analysis, intracranial aneurysm, non-parametric linkage, parametric linkage, complex genetics

وصف الملف: application/pdf

Relation: https://elischolar.library.yale.edu/ymtdl/277; https://elischolar.library.yale.edu/context/ymtdl/article/1276/viewcontent/Thesisfinal_ali_ozturk.pdf

الاتاحة: https://elischolar.library.yale.edu/ymtdl/277
https://elischolar.library.yale.edu/context/ymtdl/article/1276/viewcontent/Thesisfinal_ali_ozturk.pdf