부산대학교 도서관

Smit RAJ; Wade KH; Hui Q; Arias JD; Yin X; Christiansen MR; Yengo L; Preuss MH; Nakabuye M; Rocheleau G; Graham SE; Buchanan VL; Chittoor G; Graff M; Guindo-Martínez M; Lu Y; Marouli E; Sakaue S; Spracklen CN; Vedantam S; Wilson EP; Chen SH; Ferreira T; Ji Y; Karaderi T; Lüll K; Machado M; Malden DE; Medina-Gomez C; Moore A; Rüeger S; Akiyama M; Allison MA; Alvarez M; Andersen MK; Appadurai V; Arbeeva L; Bartell E; Bhaskar S; Bielak LF; Bis JC; Bollepalli S; Bork-Jensen J; Bradfield JP; Bradford Y; Brandl C; Braund PS; Brody JA; Broeckel U; Burgdorf KS; Cade BE; Cai Q; Camarda S; Campbell A; Cañadas-Garre M; Chai JF; Chesi A; Choi SH; Christofidou P; Couture C; Cuellar-Partida G; Danning R; Degenhardt F; Delgado GE; Delitala A; Demirkan A; Deng X; Dietl A; Dimitriou M; Dimitrov L; Dorajoo R; Eichelmann F; Eliasen AU; Engmann JE; Erdos MR; Fairhurst-Hunter Z; Farmaki AE; Faul JD; Fernandez-Lopez JC; Forer L; Frank M; Freitag-Wolf S; Fritsche LG; Fuchsberger C; Galesloot TE; Gao 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Nat Med
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23andMe Research Team 2025, ' Polygenic prediction of body mass index and obesity through the life course and across ancestries ', Nature Medicine, vol. 31, no. 9, pp. 3151-3168 . https://doi.org/10.1038/s41591-025-03827-z

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npj Genomic Medicine. 10(1)

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Commun Med (Lond)

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Nat Genet
Nature genetics
(2023).
info:cnr-pdr/source/autori:R Stevelink; C Campbell; S Chen; B Abou-Khalil; O M Adesoji; Z Afawi; E Amadori; A Anderson; J Anderson; D M Andrade; G Annesi; P Auce; A Avbersek; M Bahlo; M D Baker; G Balagura; S Balestrini; International League Against Epilepsy Consortium on Complex Epilepsies:/titolo:GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture/doi:/rivista:Nature genetics (Print)/anno:2023/pagina_da:/pagina_a:/intervallo_pagine:/volume
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Molecular Psychiatry. 30(7):3359-3359

Liu C; Department of Pediatrics, Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, United States.; Department of Biomedical Informatics, Columbia University, New York, NY 10032, United States.; Crew KD; Department of Medicine and Epidemiology, Columbia University Irving Medical Center, New York, NY 10032, United States.; Morse J; Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Linder JE; Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Antoniou AC; Department of Public Health and Primary Care, University of Cambridge, Cambridge, CB2 0SR, United Kingdom.; Carver T; Department of Public Health and Primary Care, University of Cambridge, Cambridge, CB2 0SR, United Kingdom.; Cortopassi J; Department of Neurology, University of Alabama at Birmingham, Birmingham, AL 35294, United States.; Peterson JF; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Ta CN; Department of Biomedical Informatics, Columbia University, New York, NY 10032, United States.; Hoell C; Center for Genetic Medicine, Northwestern University, Chicago, IL 60611, United States.; Prows C; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, United States.; Kenny EE; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; Miller E; Department of Personalized Medicine, Mass General Brigham, Boston, MA 02114, United States.; Perez E; Department of Personalized Medicine, Mass General Brigham, Boston, MA 02114, United States.; Jarvik GP; Departments of Medicine and Genome Sciences, University of Washington, Seattle, WA 98195, United States.; Bland HT; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Odgis JA; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; Mittendorf KF; Division of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Bonini KE; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; McGuffin K; Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Kottyan LC; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, United States.; Maradik M; Center for Genetic Medicine, Northwestern University, Chicago, IL 60611, United States.; Limdi N; Department of Neurology, University of Alabama at Birmingham, Birmingham, AL 35294, United States.; Abul-Husn NS; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; Marathe PN; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; Suckiel SA; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.; Aguilar S; Medical Affairs, Invitae Corporation, San Francisco, SF 94103, United States.; Lewis TJ; Department of Medicine, Division of Genetic Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Wei WQ; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN 37232, United States.; Luo Y; Department of Preventive Medicine, Northwestern University, Chicago, IL 60611, United States.; Freimuth RR; Department of Artificial Intelligence and Informatics, Mayo Clinic, Rochester, MN 55905, United States.; Hakonarson H; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States.; Weng C; Department of Biomedical Informatics, Columbia University, New York, NY 10032, United States.; Chung WK; Department of Pediatrics, Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, United States.; Wiesner GL; Department of Medicine, Division of Genetic Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, United States.

Publisher: Oxford University Press on behalf of the American Medical Informatics Association Country of Publication: United States NLM ID: 101730643 Publication Model: eCollection Cited Medium: Internet ISSN: 2574-2531 (Electronic) Linking ISSN: 25742531 NLM ISO Abbreviation: JAMIA Open Subsets: PubMed not MEDLINE

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Nature Genetics
EADB, GR@ACE, DEGESCO, EADI, GERAD, Demgene, FinnGen, ADGC & CHARGE 2022, 'New insights into the genetic etiology of Alzheimer's disease and related dementias', Nature Genetics, vol. 54, no. 4, pp. 412-436. https://doi.org/10.1038/s41588-022-01024-z
Nature genetics 54(4), 412-436 (2022). doi:10.1038/s41588-022-01024-z
Nature Genetics, 54, 4, pp. 412-436
Nature genetics, vol. 54, no. 4, pp. 412-436
Nature genetics
Bellenguez, C, Küçükali, F, Jansen, I E, Kleineidam, L, Moreno-Grau, S, Amin, N, Naj, A C, Campos-Martin, R, Grenier-Boley, B, Andrade, V, Holmans, P A, Boland, A, Damotte, V, van der Lee, S J, Costa, M R, Kuulasmaa, T, Yang, Q, de Rojas, I, Bis, J C, Yaqub, A, Prokic, I, Chapuis, J, Ahmad, S, Giedraitis, V, Aarsland, D, Garcia-Gonzalez, P, Abdelnour, C, Hardy, J, Morgan, K, Zhao, Y, Craig, D, Shaw, C E, Todd, S, Marín, M, Johnston, J A, Passmore, P, Daly, M, Graham, R, Gormley, P, Whelan, C, Chen, H, Wu, Y, Rice, D, King, K S, Elliott, A, Nguyen, T, Quinn, J F, Zhao, Y, Liu, X, Romero, J, McGuinness, B, EADB, GR@ACE, DEGESCO, EADI, GERAD, Demgene, FinnGen, ADGC & CHARGE 2022, 'New insights into the genetic etiology of Alzheimer’s disease and related dementias', Nature Genetics, vol. 54, no. 4, pp. 412-436. https://doi.org/10.1038/s41588-022-01024-z
2022, 'New insights into the genetic etiology of Alzheimer's disease and related dementias', Nature Genetics, vol. 54, no. 4, pp. 412-436. https://doi.org/10.1038/s41588-022-01024-z
Bellenguez, C, Küçükali, F, Jansen, I E, Kleineidam, L, Moreno-Grau, S, Amin, N, Naj, A C, Campos-Martin, R, Grenier-Boley, B, Andrade, V, Holmans, P A, Boland, A, Damotte, V, van der Lee, S J, Costa, M R, Kuulasmaa, T, Yang, Q, de Rojas, I, Bis, J C, Yaqub, A, Prokic, I, Chapuis, J, Ahmad, S, Giedraitis, V, Aarsland, D, Garcia-Gonzalez, P, Abdelnour, C, Alarcón-Martín, E, Alcolea, D, Alegret, M, Alvarez, I, Álvarez, V, Armstrong, N J, Tsolaki, A, Antúnez, C, Appollonio, I, Arcaro, M, Archetti, S, Pastor, A A, Arosio, B, Athanasiu, L, Bailly, H, Banaj, N, Baquero, M, Barral, S, Beiser, A, Nielsen, S F, Nordestgaard, B G, Sáez, M E, Frikke-Schmidt, R, EADB, GR@ACE, DEGESCO, EADI, GERAD, Demgene, FinnGen, ADGC & CHARGE 2022, ' New insights into the genetic etiology of Alzheimer's disease and related dementias ', Nature Genetics, vol. 54, no. 4, pp. 412-436 . https://doi.org/10.1038/s41588-022-01024-z
Cox, S R & Davies, G & Marioni, R E 2022, ' New insights into the genetic etiology of Alzheimer's disease and related dementias ', Nature Genetics, vol. 54, no. 4, pp. 412-436 . https://doi.org/10.1038/s41588-022-01024-z
Nat. Genet. 54, 412-436 (2022)
Nature Genetics, vol 54, iss 4

SCANDINAVIAN STUDIES; 2025, 97 3, p1-p29, 29p.

Mattingly A; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Vickery Z; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Fiorentino A; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Wilson E; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; McCune S; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Clark S; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Blanchard E; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Spencer J; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Broom A; Center for Cancer Research, Anderson University, 316 Boulevard, Anderson, SC 29621, USA.; Ivankovic D; Center for Cancer Research, Anderson University, 316 Boulevard, Anderson, SC 29621, USA.; Pace B; Center for Cancer Research, Anderson University, 316 Boulevard, Anderson, SC 29621, USA.; Baskin L; Center for Cancer Research, Anderson University, 316 Boulevard, Anderson, SC 29621, USA.; Abenavoli L; Department of Health Sciences, University 'Magna Graecia', Viale Europa-Germaneto, 88100 Catanzaro, Italy.; Edenfield WJ; Prisma Health Cancer Institute, Greenville, SC 29605, USA.; Chung K; Prisma Health Cancer Institute, Greenville, SC 29605, USA.; Farrell CL; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.; Hakonarson H; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Boccuto L; Healthcare Genetics Laboratory, School of Nursing, Clemson University, Clemson, SC 29634, USA.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101578790 Publication Model: Electronic Cited Medium: Print ISSN: 2218-1989 (Print) Linking ISSN: 22181989 NLM ISO Abbreviation: Metabolites Subsets: PubMed not MEDLINE

Meng Z; College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.; Song Y; College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.; Jiang Y; College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.; Wang X; College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.; Zou Y; School of Computer Science, Northwestern Polytechnical University, Shanxi, China.; Li X; College of Computer Science and Technology, Zhejiang University, Zhejiang, China.; Hakonarson H; Center for Applied Genomics, The Children's Hospital of Philadelphia, Pennsylvania, PA, USA. hakonarson@email.chop.edu.; Chang X; College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China. changxiao@sdfmu.edu.cn.

Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

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Nature 610 (2022): 704–712. doi:10.1038/s41586-022-05275-y
info:cnr-pdr/source/autori:Loïc Yengo # 1, Sailaja Vedantam # 2 3, Eirini Marouli # 4, Julia Sidorenko 5, Eric Bartell 2 3 6, Saori Sakaue 3 7 8 9, Marielisa Graff 10, Anders U Eliasen 11 12, Yunxuan Jiang 13, Sridharan Raghavan 14 15, Jenkai Miao 2 3, Joshua D Arias 16, Sarah E Graham 17, Ronen E Mukamel 3 18 19, Cassandra N Spracklen 20 21, Xianyong Yin 22, Shyh-Huei Chen 23, Teresa Ferreira 24, Heather H Highland 10, Yingjie Ji 25, Tugce Karaderi 26 27, Kuang Lin 28, Kreete Lüll 29, Deborah E Malden 28, Carolina Medina-Gomez 30, Moara Machado 16, Amy Moore 31, Sina Rüeger 32 33, Xueling Sim 34, Scott Vrieze 35, Tarunveer S Ahluwalia 36 37, Masato Akiyama 7 38, Matthew A Allison 39, Marcus Alvarez 40, Mette K Andersen 41, Alireza Ani 42 43, Vivek Appadurai 44, Liubov Arbeeva 45, Seema Bhaskar 46, Lawrence F Bielak 47, Sailalitha Bollepalli 48, Lori L Bonnycastle 49, Jette Bork-Jensen 41, Jonathan P Bradfield 50 51, Yuki Bradford 52, Peter S Braund 53 54, Jennifer A Brody 55, Kristoffer S Burgdorf 56 57, Brian E Cade 6 58, Hui Cai 59, Qiuyin Cai 59, Archie Campbell 60, Marisa Cañadas-Garre 61, Eulalia Catamo 62, Jin-Fang Chai 34, Xiaoran Chai 63 64, Li-Ching Chang 65, Yi-Cheng Chang 65 66 67, Chien-Hsiun Chen 65, Alessandra Chesi 68 69, Seung Hoan Choi 70, Ren-Hua Chung 71, Massimiliano Cocca 62, Maria Pina Concas 62, Christian Couture 72, Gabriel Cuellar-Partida 13 73, Rebecca Danning 74, E Warwick Daw 75, Frauke Degenhard 76, Graciela E Delgado 77, Alessandro Delitala 78, Ayse Demirkan 79 80, Xuan Deng 81, Poornima Devineni 82, Alexander Dietl 83 84, Maria Dimitriou 85, Latchezar Dimitrov 86, Rajkumar Dorajoo 87 88, Arif B Ekici 89, Jorgen E Engmann 90, Zammy Fairhurst-Hunter 28, Aliki-Eleni Farmaki 85, Jessica D Faul 91, Juan-Carlos Fernandez-Lopez 92, Lukas Forer 93, Margherita Francescatto 94, Sandra Freitag-Wolf 95, Christian Fuchsberger 96, Tessel E Galesloot 97, Yan Gao 98, Zishan Gao 99 100 101, Frank Geller 102, Olga Giannakopoulou 4, Franco Giulianini 74, Anette P Gjesing 41, Anuj Goel 27 103, Scott D Gordon 104, Mathias Gorski 83, Jakob Grove 105 106 107, Xiuqing Guo 108, Stefan Gustafsson 109, Jeffrey Haessler 110, Thomas F Hansen 44 57 111, Aki S Havulinna 48 112, Simon J Haworth 113 114, Jing He 59, Nancy Heard-Costa 115 116, Prashantha Hebbar 117, George Hindy 3 118, Yuk-Lam A Ho 119, Edith Hofer 120 121, Elizabeth Holliday 122, Katrin Horn 123 124, Whitney E Hornsby 17, Jouke-Jan Hottenga 125, Hongyan Huang 126, Jie Huang 127 128, Alicia Huerta-Chagoya 129 130 131, Jennifer E Huffman 119, Yi-Jen Hung 132, Shaofeng Huo 133, Mi Yeong Hwang 134, Hiroyuki Iha 135, Daisuke D Ikeda 135, Masato Isono 136, Anne U Jackson 22, Susanne Jäger 137 138, Iris E Jansen 139 140, Ingegerd Johansson 141 142, Jost B Jonas 143 144 145 146, Anna Jonsson 41, Torben Jørgensen 147 148, Ioanna-Panagiota Kalafati 85, Masahiro Kanai 3 7 8, Stavroula Kanoni 4, Line L Kårhus 147, Anuradhani Kasturiratne 149, Tomohiro Katsuya 150, Takahisa 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Mitsuhiro Yokota 479, Jian-Min Yuan 480 481, Eleftheria Zeggini 216 233 482, Babette S Zemel 52 69 340 343, Wei Zheng 59, Xiaofeng Zhu 167, Joseph M Zmuda 481, Alan B Zonderman 225, John-Anker Zwart 256 483 ; 23andMe Research Team; VA Million Veteran Program; DiscovEHR (DiscovEHR and MyCode Community Health Initiative); eMERGE (Electronic Medical Records and Genomics Network); Lifelines Cohort Study; PRACTICAL Consortium; Understanding Society Scientific Group; Daniel I Chasman 6 74, Yoon Shin Cho 226, Iris M Heid 83, Mark I McCarthy 27 217 484, Maggie C Y Ng 86 485, Christopher J O'Donnell 6 58 486, Fernando Rivadeneira 30, Unnur Thorsteinsdottir 234 341, Yan V Sun 487 488, E Shyong Tai 34 466, Michael Boehnke 22, Panos Deloukas 4 489, Anne E Justice 10 490, Cecilia M Lindgren 3 24 27, Ruth J F Loos 41 210 211 491, Karen L Mohlke 20, Kari E North 10, Kari Stefansson 234 341, Robin G Walters 28 193, Thomas W Winkler 83, Kristin L Young 10, Po-Ru Loh 3 18 19, Jian Yang 5 492 493, Tõnu 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eMERGE (Electronic Medical Records and Genomics Network), The PRACTICAL consortium, Lifelines Cohort Study, 23andMe Research team, Understanding Society Scientific group, VA Million Veteran Program & DiscovEHR (DiscovEHR and MyCode Community Health Initiative) 2022, 'A saturated map of common genetic variants associated with human height', Nature, vol. 610, pp. 704-712. https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610, 7933, pp. 704-712
Nature, vol. 610, no. 7933, pp. 704-712
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Andersen, M K, Grove, J, Hansen, T F, Jørgensen, T, Mattheisen, M, Petersen, L V, Wang, Z, Børglum, A D, Dantoft, T M, Grarup, N, Hansen, T, Huang, W, Nielsen, C S, Pedersen, O, Ng, M C Y, Sun, Y V, Winkler, T W, Yang, J, 23andMe Research Team, VA Million Vet Program, DiscovEHR Collaboration, eMERGE Consortium, Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, 'A saturated map of common genetic variants associated with human height', Nature, vol. 610, no. 7933, pp. 704–712. https://doi.org/10.1038/s41586-022-05275-y
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Allison, M A, Alvarez, M, Andersen, M K, Ani, A, Appadurai, V, Arbeeva, L, Cai, H, Cañadas-Garre, M, Li, X, Nelson, C P, Smyth, L J, Sun, L, Wang, Z, Cole, J W, Cooper, R S, Kee, F, McKnight, A J, Weir, D R & 23andMe Research Team 2022, 'A saturated map of common genetic variants associated with human height', Nature. https://doi.org/10.1038/s41586-022-05275-y
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lull, K, Malden, D E, Andersen, M K, Appadurai, V, Bork-Jensen, J, Burgdorf, K S, Hansen, T F, Jonsson, A, Jorgensen, T, Liu, J, Mollehave, L T, Smit, R A J, Zhao, J-H, Bisgaard, H, Bonnelykke, K, Dantoft, T M, Grarup, N, Hansen, T, Jackson, R D, Karpe, F, Kovacs, P, Lind, L, Linneberg, A, Pedersen, O, Werge, T M, Sun, Y, Loos, R J F, Winkler, T W, 23andMe Res Team, VA Million Vet Program, DiscovEHR DiscovEHR MyCode Communi, eEMERGE Elect Med Records Genomics, LifeLines Cohort Study, PRACTICAL consortium & Understanding Soc Sci Grp 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y

Biglari S; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Youssefian L; Department of Pathology, Cytogenetics Laboratory, City of Hope National Medical Center, Irwindale, CA, USA.; Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Saeidian AH; Center for Applied Genomics, Children'S Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Abtahi-Naeini B; Pediatric Dermatology Division, Department of Pediatrics, Imam Hossein Children'S Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.; Skin Diseases and Leishmaniasis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Khorram E; Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.; Sherkat R; Immunodeficiency Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Moghaddam AS; Department of Genetics, Faculty of Biological Science, North Tehran Branch, Islamic Azad University, Tehran, Iran.; Mohaghegh F; Department of Dermatology, Skin Diseases and Leishmaniasis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Rahimi M; Pediatrics Department, Isfahan University of Medical Sciences, Isfahan, Iran.; Rahimi H; Pediatric Infectious Diseases Department, Isfahan University of Medical Sciences, Isfahan, Iran.; Babaei S; Department of Asthma, Allergy and Clinical Immunology, Child Growth and Development Research Center, Research Institute of Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.; Shahrooei M; Dr. Shahrooei Laboratory, Tehran, Iran.; Clinical and Diagnostic Immunology, 3000, Louvain, KU, Belgium.; Mozafari N; Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Zaresharifi S; Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Vahidnezhad F; Department of Computer Science and Engineering Technology, University of Maryland Eastern Shore, Princess Anne, MD, USA.; Homayouni V; Immunodeficiency Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Tsoi LC; Department of Dermatology, University of Michigan, Ann Arbor, MI, 48109, USA.; Gudjonsson JE; Department of Dermatology, University of Michigan, Ann Arbor, MI, 48109, USA.; Hakonarson H; Center for Applied Genomics, Children'S Hospital of Philadelphia, Philadelphia, PA, USA.; Division of Human Genetics, Children'S Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.; Casanova JL; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, Inserm U1163, Paris, France.; Imagine Institute, Paris Cité University, Paris, France.; Department of Pediatrics, Necker Hospital for Sick Children, Paris, EU, France.; Howard Hughes Medical Institute, Chevy Chase, MD, 20815, USA.; Jouanguy E; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, Inserm U1163, Paris, France.; Imagine Institute, Paris Cité University, Paris, France.; Béziat V; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, Inserm U1163, Paris, France.; Imagine Institute, Paris Cité University, Paris, France.; Zhang Q; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, Inserm U1163, Paris, France.; Imagine Institute, Paris Cité University, Paris, France.; Cobat A; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker Hospital for Sick Children, Inserm U1163, Paris, France.; Imagine Institute, Paris Cité University, Paris, France.; Vahidnezhad H; Center for Applied Genomics, Children'S Hospital of Philadelphia, Philadelphia, PA, USA. Vahidnezhh@chop.edu.; Division of Human Genetics, Children'S Hospital of Philadelphia, Philadelphia, PA, USA. Vahidnezhh@chop.edu.; Department of Pediatrics, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA. Vahidnezhh@chop.edu.; Department of Dermatology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA. Vahidnezhh@chop.edu.

Publisher: Springer Country of Publication: Netherlands NLM ID: 8102137 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-2592 (Electronic) Linking ISSN: 02719142 NLM ISO Abbreviation: J Clin Immunol Subsets: MEDLINE

Snorradottir AO; Faculty of Medicine, University of Iceland, Reykjavik, Iceland. asbjorgosk@hi.is.; Department of Pathology, Landspitali - The National University Hospital of Iceland, Reykjavik, Iceland. asbjorgosk@hi.is.; Arctic Therapeutics, Bjargargata 1, Reykjavik, Iceland. asbjorgosk@hi.is.; Hafsteinsson HK; Department of Pathology, Landspitali - The National University Hospital of Iceland, Reykjavik, Iceland.; Hansdottir K; Department of Pathology, Landspitali - The National University Hospital of Iceland, Reykjavik, Iceland.; Ingþorsson S; Faculty of Nursing and Midwifery, University of Iceland, Reykjavik, Iceland.; Biomedical Center, School of Health Sciences, University of Iceland, Reykjavik, Iceland.; Gudmundsson SR; Biomedical Center, School of Health Sciences, University of Iceland, Reykjavik, Iceland.; Skodras A; Department of Cellular Neurology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; Isaksson HJ; Department of Pathology, Landspitali - The National University Hospital of Iceland, Reykjavik, Iceland.; Hakonarson H; Faculty of Medicine, University of Iceland, Reykjavik, Iceland.; Arctic Therapeutics, Bjargargata 1, Reykjavik, Iceland.; Center for Applied Genomics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2051-5960 (Electronic) Linking ISSN: 20515960 NLM ISO Abbreviation: Acta Neuropathol Commun Subsets: MEDLINE

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