المؤلفون: Belanger, Janelle M, Heinonen, Tiina, Famula, Thomas R, Mandigers, Paul JJ, Leegwater, Peter A, Hytönen, Marjo K, Lohi, Hannes, Oberbauer, Anita M

المصدر: Genes. 13(7)

مصطلحات موضوعية: Biological Sciences, Genetics, Neurosciences, Brain Disorders, Human Genome, Biotechnology, Rare Diseases, Epilepsy, Neurodegenerative, Aetiology, 2.1 Biological and endogenous factors, Animals, Belgium, Dog Diseases, Dogs, Genetic Predisposition to Disease, Haplotypes, Humans, ras Guanine Nucleotide Exchange Factors, dog, idiopathic epilepsy, RAPGEF5, risk haplotype

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1dd8q7ft
https://escholarship.org/content/qt1dd8q7ft/qt1dd8q7ft.pdf

المؤلفون: Benzow, Kellie, Karanjeet, Kul, Oblak, Adrian L., Carter, Gregory W., Sasner, Michael, Koob, Michael D.

المساهمون: Radiology and Imaging Sciences, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Functional sequence variant, Gene‐replacement mouse model, Protective haplotype, Risk haplotype

وصف الملف: application/pdf

Relation: Alzheimer's & Dementia; Benzow K, Karanjeet K, Oblak AL, Carter GW, Sasner M, Koob MD. Gene replacement-Alzheimer's disease (GR-AD): Modeling the genetics of human dementias in mice. Alzheimers Dement. 2024;20(4):3080-3087. doi:10.1002/alz.13730; https://hdl.handle.net/1805/42172

الاتاحة: https://hdl.handle.net/1805/42172

المؤلفون: Humberto García-Ortiz, Francisco Barajas-Olmos, Marlen Flores-Huacuja, Monserrat I. Morales-Rivera, Angélica Martínez-Hernández, Vicente Baca, Cecilia Contreras-Cubas, Lorena Orozco

المصدر: Frontiers in Medicine, Vol 9 (2023)

مصطلحات موضوعية: childhood-onset systemic lupus erythematosus, Xq28 risk haplotype, ancestry-dependent, IRAK1, MECP2, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fmed.2022.1044856/full; https://doaj.org/toc/2296-858X

URL الوصول: https://doaj.org/article/8b62430afbe34f46aa3878d9b9209a33

المؤلفون: Tschernoster, Nikolai, Erger, Florian, Kohl, Stefan, Reusch, Björn, Wenzel, Andrea, Walsh, Stephen, Thiele, Holger, Becker, Christian, Franitza, Marek, Bartram, Malte P., Kömhoff, Martin, Schumacher, Lena, Kukat, Christian, Borodina, Tatiana, Quedenau, Claudia, Nürnberg, Peter, Rinschen, Markus M., Driller, Jan H., Pedersen, Bjørn P., Schlingmann, Karl P., Hüttel, Bruno, Bockenhauer, Detlef, Beck, Bodo, Altmüller, Janine

المصدر: Tschernoster , N , Erger , F , Kohl , S , Reusch , B , Wenzel , A , Walsh , S , Thiele , H , Becker , C , Franitza , M , Bartram , M P , Kömhoff , M , Schumacher , L , Kukat , C , Borodina , T , Quedenau , C , Nürnberg , P , Rinschen , M M , Driller , J H , Pedersen , B P , Schlingmann , K P , Hüttel , B , Bockenhauer , D , Beck , B & Altmüller , ....

مصطلحات موضوعية: Bartter syndrome type 3, CLCNKA, CLCNKB, HiFi-sequencing, Long-read sequencing, Next-generation sequencing, Risk haplotype, Salt-wasting tubulopathy, Structural variant, Target enrichment

Relation: https://pure.au.dk/portal/en/publications/53efb788-2420-4d57-8613-b7821ec186cc

الاتاحة: https://pure.au.dk/portal/en/publications/53efb788-2420-4d57-8613-b7821ec186cc
https://doi.org/10.1186/s13073-023-01215-1
http://www.scopus.com/inward/record.url?scp=85168624869&partnerID=8YFLogxK

المؤلفون: Jiao, Xiang, Aravidis, Christos, Marikkannu, Rajeshwari, Rantala, Johanna, Picelli, Simone, Adamovic, Tatjana, Liu, Tao, Maguire, Paula, Kremeyer, Barbara, Luo, Liping, von Holst, Susanna, Kontham, Vinaykumar, Thutkawkorapin, Jessada, Margolin, Sara, Du, Quan, Lundin, Johanna, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Lush, Michael, Ambrosone, Christine B, Andrulis, Irene L, Anton-Culver, Hoda, Antonenkova, Natalia N, Arndt, Volker, Beckmann, Matthias W, Blomqvist, Carl, Blot, William, Boeckx, Bram, Bojesen, Stig E, Bonanni, Bernardo, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Broeks, Annegien, Brüning, Thomas, Burwinkel, Barbara, Cai, Qiuyin, Chang-Claude, Jenny, Couch, Fergus J, Cox, Angela, Cross, Simon S, Deming-Halverson, Sandra L, Devilee, Peter, dos-Santos-Silva, Isabel, Dörk, Thilo, Eriksson, Mikael, Fasching, Peter A, Figueroa, Jonine, Flesch-Janys, Dieter, Flyger, Henrik, Gabrielson, Marike, García-Closas, Montserrat, Giles, Graham G, González-Neira, Anna, Guénel, Pascal, Guo, Qi, Gündert, Melanie, Haiman, Christopher A, Hallberg, Emily, Hamann, Ute, Harrington, Patricia, Hooning, Maartje J, Hopper, John L, Huang, Guanmengqian, Jakubowska, Anna, Jones, Michael E, Kerin, Michael J, Kosma, Veli-Matti, Kristensen, Vessela N, Lambrechts, Diether, Le Marchand, Loic, Lubinski, Jan, Mannermaa, Arto, Martens, John WM, Meindl, Alfons, Milne, Roger L, Mulligan, Anna Marie, Neuhausen, Susan L, Nevanlinna, Heli, Peto, Julian, Pylkäs, Katri, Radice, Paolo, Rhenius, Valerie, Sawyer, Elinor J, Schmidt, Marjanka K, Schmutzler, Rita K, Seynaeve, Caroline, Shah, Mitul, Simard, Jacques, Southey, Melissa C, Swerdlow, Anthony J, Truong, Thérèse, Wendt, Camilla, Winqvist, Robert, Zheng, Wei, Benitez, Javier, Dunning, Alison M, Pharoah, Paul DP

المصدر: Oncotarget. 8(61)

مصطلحات موضوعية: Cancer, Prevention, Breast Cancer, Genetics, Human Genome, Genetic Testing, 2.1 Biological and endogenous factors, Aetiology, familial breast cancer, linkage analysis, risk haplotype, sequencing, NBCS Collaborators, kConFab/AOCS Investigators, Oncology and Carcinogenesis

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6gx4c4wc

المؤلفون: Stefano Mocci, Roberto Littera, Stefania Tranquilli, Aldesia Provenzano, Alessia Mascia, Federica Cannas, Sara Lai, Erika Giuressi, Luchino Chessa, Goffredo Angioni, Marcello Campagna, Davide Firinu, Maria Del Zompo, Giorgio La Nasa, Andrea Perra, Sabrina Giglio

المصدر: Frontiers in Immunology, Vol 13 (2022)

مصطلحات موضوعية: COVID-19, SARS-CoV-2, Neanderthal Covid-19 risk haplotype, rs35044562 variant, HLA-A*02:01, B*18:01, Immunologic diseases. Allergy, RC581-607

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fimmu.2022.891147/full; https://doaj.org/toc/1664-3224

URL الوصول: https://doaj.org/article/bd45465770fa42918eb39b483da90837

المؤلفون: Nataliia Karpova, Olga Dmitrenko, Ekaterina Arshinova

المصدر: Biology and Life Sciences Forum; Volume 20; Issue 1; Pages: 31

مصطلحات موضوعية: preeclampsia SNP, polymorphism, FLT1, risk haplotype, TFBs, TF

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/IECBM2022-13721

الاتاحة: https://doi.org/10.3390/IECBM2022-13721

المؤلفون: Krishnamoorthy Srikanth, Dirsko J. F. von Pfeil, Bryden J. Stanley, Caroline Griffitts, Heather J. Huson

المصدر: Genes; Volume 13; Issue 10; Pages: 1808

مصطلحات موضوعية: congenital laryngeal paralysis, Alaskan sled dog, Alaskan husky, GWAS, WGS, risk haplotype, CFA18, ALX4, EXT2, TSPAN53I11

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Animal Genetics and Genomics; https://dx.doi.org/10.3390/genes13101808

الاتاحة: https://doi.org/10.3390/genes13101808

المؤلفون: Janelle M. Belanger, Tiina Heinonen, Thomas R. Famula, Paul J. J. Mandigers, Peter A. Leegwater, Marjo K. Hytönen, Hannes Lohi, Anita M. Oberbauer

المصدر: Genes; Volume 13; Issue 7; Pages: 1124

مصطلحات موضوعية: dog, idiopathic epilepsy, RAPGEF5, risk haplotype

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Animal Genetics and Genomics; https://dx.doi.org/10.3390/genes13071124

الاتاحة: https://doi.org/10.3390/genes13071124

المؤلفون: Mel·lina Pinsach-Abuin, Bernat del Olmo, Adrian Pérez-Agustin, Jesus Mates, Catarina Allegue, Anna Iglesias, Qi Ma, Daria Merkurjev, Sergiy Konovalov, Jing Zhang, Farah Sheikh, Amalio Telenti, Josep Brugada, Ramon Brugada, Melissa Gymrek, Julia di Iulio, Ivan Garcia-Bassets, Sara Pagans

المصدر: Cell Reports Medicine, Vol 2, Iss 4, Pp 100250- (2021)

مصطلحات موضوعية: GWAS, haplotype block, common SNV, non-coding SNV, SNV redundancy, risk haplotype, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666379121000665; https://doaj.org/toc/2666-3791

URL الوصول: https://doaj.org/article/6c838ad5069a44029f4b3ea3f35643c1

المؤلفون: Harald Prüss, Guido Gessner, Stefan H. Heinemann, Franz Rüschendorf, Ann-Kathrin Ruppert, Herbert Schulz, Thomas Sander, Wilhelm Rimpau

المصدر: Frontiers in Neurology, Vol 10 (2019)

مصطلحات موضوعية: LQT syndrome, KCNQ1, familial epilepsy, risk haplotype, genetic modifier, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fneur.2019.00648/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/3cefa7166a1c4a8eb67dbab21883cf8b

المؤلفون: Bandres-Ciga, Sara, Sarah, Ahmed, Marya S., Sabir, Blauwendraat, Cornelis, Adarmes-Gómez, Astrid D, Bernal-Bernal, Inmaculada, Bonilla-Toribio, Marta, Buiza-Rueda, Dolores, Carrillo, Fátima, Carrión-Claro, Mario, Gómez Garre, Pilar, Jesús, Silvia, Labrador-Espinosa, Miguel A., Macías, Daniel, Méndez-del-Barrio, Carlota, Periñán-Tocino, Teresa, Tejera-Parrado, Cristina, Vargas González, Laura, Diez-Fairen, Monica, Alvarez, Ignacio, Tartari, Juan Pablo, Buongiorno, Mariateresa, Aguilar, Miguel, Gorostidi, Ana, Bergareche, Jesús Alberto, Mondragon, Elisabet, Vinagre-Aragon, Ana, Croitoru, Ioana, Ruiz-Martínez, Javier, Dols-Icardo, Oriol, Kulisevsky, Jaime, Marín-Lahoz, Juan, Pagonabarraga, Javier, Pascual-Sedano, Berta, Ezquerra, Mario, Cámara, Ana, Compta, Yaroslau, Fernández, Manel, Fernández-Santiago, Rubén, Muñoz, Estaban, Tolosa, Eduard, Valldeoriola, Francesc, Gonzalez-Aramburu, Isabel, Sanchez Rodriguez, Antonio, Sierra, Maria, Menéndez-González, Manuel, Blazquez, Marta, García, Ciara, Suarez-San Martin, Esther, García-Ruiz, Pedro, Martínez-Castrillo, Juan Carlos, Vela-Desojo, Lydia, Ruz, Clara, Barrero Hernández, Francisco Javier, Escamilla-Sevilla, Francisco, Mínguez-Castellanos, Adolfo, Cerdan, Debora, Tabernero, Cesar, Gómez Heredia, Maria José, Pérez Errazquin, Francisco, Romero Acebal, Manuel, Feliz, Cici, Lopez-Sendon, Jose Luis, Mata, Marina, Martínez Torres, Irene, Kim, Jonggeol Jeffrey, Dalgard, Clifton L, Brooks, Janet, Saez- SaezAtienzar, Sara, Gibbs, J. Raphael, Jorda, Rafael, Botia, Juan A, Bonet-Ponce, Luis, Morrison, Karen E, Clarke, Carl, Tan, Manuela, Morris, Huw, Edsall, Connor, Hernandez, Dena, Simón-Sanchez, Javier, Nalls, Mike A, Scholz, Sonja W, Jimenez-Escrig, Adriano, Duarte, Jacinto, Vives Montero, Francisco, Durán Ogalla, Raquel, Hoenicka, Janet, Álvarez, Victoria, Infante, Jon, Marti, Maria Jose, Clarimón, Jordi, Lopez De Munain, Adolfo, Pastor, Pau, Singleton, Andrew

مصطلحات موضوعية: Age at onset, Parkinson’s disease, Polygenic risk score, Risk haplotype, Spanish population

Relation: Published version: Bandres-Ciga S, et al. International Parkinson Disease Genomics Consortium. The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight. Mov Disord. 2019 Dec;34(12):1851-1863. Epub 2019 Oct 29. PMID: 31660654; PMCID: PMC8393828. doi:10.1002/mds.27864; https://hdl.handle.net/10481/90874

الاتاحة: https://hdl.handle.net/10481/90874
https://doi.org/10.1002/mds.27864

المؤلفون: Raha-Chowdhury, Ruma, Henderson, James W, Raha, Animesh Alexander, Vuono, Romina, Bickerton, Anastasia, Jones, Elizabeth, Fincham, Robert, Allinson, Kieren, Holland, Anthony, Zaman, Shahid H

مصطلحات موضوعية: Alzheimer’s disease, Down syndrome, TREM2, blood-CSF barrier, blood-brain barrier, choroid plexus, high-risk haplotype, neuroinflammation, tau trafficking, white matter tract

وصف الملف: application/pdf

Relation: https://www.repository.cam.ac.uk/handle/1810/293194

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/293194
https://doi.org/10.17863/CAM.40344

المؤلفون: Prüss, Harald, Gessner, Guido, Heinemann, Stefan H., Rüschendorf, Franz, Ruppert, Ann-Katrin, Schulz, Herbert, Sander, Thomas, Rimpau, Wilhelm

مصطلحات موضوعية: KCNQ1, LQT syndrome, familial epilepsy, genetic modifier, risk haplotype, ddc:610

وصف الملف: application/pdf

Relation: https://refubium.fu-berlin.de/handle/fub188/25151; http://dx.doi.org/10.17169/refubium-2906

الاتاحة: https://refubium.fu-berlin.de/handle/fub188/25151
https://doi.org/10.17169/refubium-2906
https://doi.org/10.3389/fneur.2019.00648

المؤلفون: Humberto García-Ortiz (3129330), Francisco Barajas-Olmos (3129315), Marlen Flores-Huacuja (14192986), Monserrat I. Morales-Rivera (14392608), Angélica Martínez-Hernández (586073), Vicente Baca (14392611), Cecilia Contreras-Cubas (733421), Lorena Orozco (180145)

مصطلحات موضوعية: Dermatology, Emergency Medicine, Gastroenterology and Hepatology, Geriatrics and Gerontology, Intensive Care, Medical Genetics (excl. Cancer Genetics), Nephrology and Urology, Nuclear Medicine, Orthopaedics, Otorhinolaryngology, Pathology (excl. Oral Pathology), Radiology and Organ Imaging, Foetal Development and Medicine, Obstetrics and Gynaecology, Family Care, Primary Health Care, Medical and Health Sciences not elsewhere classified, childhood-onset systemic lupus erythematosus, Xq28 risk haplotype, ancestry-dependent, IRAK1, MECP2

Relation: https://figshare.com/articles/dataset/Table_1_Ancestry-dependent_genetic_structure_of_the_Xq28_risk_haplotype_in_the_Mexican_population_and_its_association_with_childhood-onset_systemic_lupus_erythematosus_docx/21876156

الاتاحة: https://doi.org/10.3389/fmed.2022.1044856.s001

المؤلفون: Jiao, Xiang, Aravidis, Christos, Marikkannu, Rajeshwari, Rantala, Johanna, Picelli, Simone, Adamovic, Tatjana, Liu, Tao, Maguire, Paula, Kremeyer, Barbara, Luo, Liping, Von Holst, Susanna, Kontham, Vinaykumar, Thutkawkorapin, Jessada, Margolin, Sara, Du, Quan, Lundin, Johanna, Michailidou, Kyriaki, Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Lush, Michael, Ambrosone, Christine B., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Arndt, Volker, Beckmann, Matthias W., Blomqvist, Carl, Blot, William, Boeckx, Bram, Bojesen, Stig E., Bonanni, Bernardo, Brand, Judith S., Brauch, Hiltrud, Brenner, Hermann, Broeks, Annegien, Bruning, Thomas, Burwinkel, Barbara, Cai, Qiuyin, Chang-Claude, Jenny, Couch, Fergus J., Cox, Angela, Cross, Simon S., Deming-Halverson, Sandra L., Devilee, Peter, dos-Santos-Silva, Isabel, Dork, Thilo, Eriksson, Mikael, Fasching, Peter A., Nevanlinna, Heli, NBCS Collaborators, kConFab-AOCS Investigators

المساهمون: Department of Oncology, Clinicum, University of Helsinki, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, HUS Comprehensive Cancer Center

مصطلحات موضوعية: familial breast cancer, linkage analysis, risk haplotype, sequencing, DNA-SEQUENCING DATA, WIDE LINKAGE SCAN, GENOME, MUTATIONS, FAMILIES, GENE, ASSOCIATION, EXPRESSION, LOCALIZATION, DISCOVERY, Cancers, Gynaecology and paediatrics

وصف الملف: application/pdf

Relation: The study was supported by grants provided by the Swedish Cancer Society (Cancerfonden), the Stockholm County Council (ALF project), the Swedish Research Council (Vetenskapsradet), the Stockholm Cancer Society (Radiumhemsfonderna) and Bert von Kantzows and Nilsson-Ehle's foundations. BCAC is funded by Cancer Research UK (C1287/A16563, C1287/A10118), the European Union's Horizon 2020 Research and Innovation Programme (grant numbers 634935 and 633784 for BRIDGES and B-CAST respectively), and by the European Community's Seventh Framework Programme under grant agreement number 223175 (grant number HEALTH-F2-2009-223175) (COGS). Funding for the iCOGS infrastructure came from: the European Community's Seventh Framework Programme under grant agreement no 223175 (HEALTH-F2-2009-223175) (COGS), Cancer Research UK (C1287/A10118, C1287/A10710, C12292/A11174, C1281/A12014, C5047/A8384, C5047/A15007, C5047/A10692, C8197/A16565), the National Institutes of Health (CA128978) and Post-Cancer GWAS initiative (1U19 CA148537, 1U19 CA148065 and 1U19 CA148112 - the GAME-ON initiative), the Department of Defence (W81XWH-10-1-0341), the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer, Komen Foundation for the Cure, the Breast Cancer Research Foundation, and the Ovarian Cancer Research Fund. Funding of individual BCAC studies is listed in the Supplemental Note.; Jiao , X , Aravidis , C , Marikkannu , R , Rantala , J , Picelli , S , Adamovic , T , Liu , T , Maguire , P , Kremeyer , B , Luo , L , Von Holst , S , Kontham , V , Thutkawkorapin , J , Margolin , S , Du , Q , Lundin , J , Michailidou , K , Bolla , M K , Wang , Q , Dennis , J , Lush , M , Ambrosone , C B , Andrulis , I L , Anton-Culver , H , Antonenkova , N N , Arndt , V , Beckmann , M W , Blomqvist , C , Blot , W , Boeckx , B , Bojesen , S E , Bonanni , B , Brand , J S , Brauch , H , Brenner , H , Broeks , A , Bruning , T , Burwinkel , B , Cai , Q , Chang-Claude , J , Couch , F J , Cox , A , Cross , S S , Deming-Halverson , S L , Devilee , P , dos-Santos-Silva , I , Dork , T , Eriksson , M , Fasching , P A , Nevanlinna , H , NBCS Collaborators & kConFab-AOCS Investigators 2017 , ' PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1 ' , Oncotarget , vol. 8 , no. 61 , pp. 102769-102782 . https://doi.org/10.18632/oncotarget.21800; http://hdl.handle.net/10138/232516; 50e98fd9-61b9-46ec-892d-48cbe5ec266b; 85035357496; 000419562500006

الاتاحة: http://hdl.handle.net/10138/232516

المؤلفون: Rintala, A, Riikonen, I, Toivonen, A, Pietilä, S, Munukka, E, Pursiheimo, JP, Elo, LL, Arikoski, P, Luopajärvi, K, Schwab, U, Uusitupa, M, Heinonen, S, Savilahti, E, Eerola, E, Ilonen, J

المساهمون: School of Medicine / Clinical Medicine, School of Medicine / Clinical Nutrition

مصطلحات موضوعية: celiac disease, HLA risk haplotype, fecal microbiota, next-generation sequencing, 16S rRNA gene sequencing

وصف الملف: 403-409

Relation: SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY; http://dx.doi.org/10.1080/00365521.2018.1444788; 53; https://erepo.uef.fi/handle/123456789/6637

الاتاحة: https://erepo.uef.fi/handle/123456789/6637

المؤلفون: Jiao, X, Easton, DF

مصطلحات موضوعية: familial breast cancer, linkage analysis, risk haplotype, sequencing

وصف الملف: application/pdf

Relation: https://www.repository.cam.ac.uk/handle/1810/271118

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/271118
https://doi.org/10.17863/CAM.18092

المؤلفون: Mocci, Stefano

مصطلحات موضوعية: COVID-19, Neanderthal Covid-19 risk haplotype, rs35044562 variant, Sardinia

Relation: https://doi.org/10.5281/zenodo.6416857; https://doi.org/10.5281/zenodo.6416858; oai:zenodo.org:6416858

الاتاحة: https://doi.org/10.5281/zenodo.6416858

المؤلفون: Stefano Mocci, Roberto Littera, Stefania Tranquilli, Aldesia Provenzano, Alessia Mascia, Federica Cannas, Sara Lai, Erika Giuressi, Luchino Chessa, Goffredo Angioni, Marcello Campagna, Davide Firinu, Maria Del Zompo, Giorgio La Nasa, Andrea Perra, Sabrina Giglio

مصطلحات موضوعية: Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, COVID-19, SARS-CoV-2, Neanderthal Covid-19 risk haplotype, rs35044562 variant, HLA-A*02:01, B*18:01, DRB*03 extended haplotype

Relation: https://figshare.com/articles/dataset/DataSheet_1_A_Protective_HLA_Extended_Haplotype_Outweighs_the_Major_COVID-19_Risk_Factor_Inherited_From_Neanderthals_in_the_Sardinian_Population_docx/19615203

الاتاحة: https://doi.org/10.3389/fimmu.2022.891147.s001
https://figshare.com/articles/dataset/DataSheet_1_A_Protective_HLA_Extended_Haplotype_Outweighs_the_Major_COVID-19_Risk_Factor_Inherited_From_Neanderthals_in_the_Sardinian_Population_docx/19615203