Rare Variants of IFIH1 , a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442

Genome sequencing in microfabricated high-density picolitre reactors

Margulies, M., Egholm, M., Altman, W. E., Attiya, S., Bader, J. S., Bemben, L. A., Berka, J., Braverman, M. S., Chen, Y.-J., Chen, Z., et al. (2005) · Nature · doi:10.1038/nature03959 · Cited by 7,693

Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses

Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K. J., et al. (2006) · Nature · doi:10.1038/nature04734 · Cited by 3,888

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

McCarthy, M. I., Abecasis, G. R., Cardon, L. R., Goldstein, D. B., Little, J., Ioannidis, J. P. A., & Hirschhorn, J. N. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2344 · Cited by 2,891

The impact of next-generation sequencing technology on genetics

Mardis, E. R. (2008) · Trends in Genetics · doi:10.1016/j.tig.2007.12.007 · Cited by 2,113

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Finland, G. O. T. 1. D. I., Todd, J. A., the Wellcome Trust Case Control Consortium, Walker, N. M., Cooper, J. D., Smyth, D. J., Downes, K., Plagnol, V., Bailey, R., Nejentsev, S., et al. (2007) · Nature Genetics · doi:10.1038/ng2068 · Cited by 1,456

Genetic Mapping in Human Disease

Altshuler, D., Daly, M. J., & Lander, E. S. (2008) · Science · doi:10.1126/science.1156409 · Cited by 1,452

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

Bottini, N., Musumeci, L., Alonso, A., Rahmouni, S., Nika, K., Rostamkhani, M., MacMurray, J. P., Meloni, T., Lucarelli, P., Pellecchia, M., et al. (2004) · Nature Genetics · doi:10.1038/ng1323 · Cited by 1,419

Intracellular pattern recognition receptors in the host response

Meylan, E., Tschopp, J., & Karin, M. (2006) · Nature · doi:10.1038/nature04946 · Cited by 1,196

Common and rare variants in multifactorial susceptibility to common diseases

Bodmer, W., & Bonilla, C. (2008) · Nature Genetics · doi:10.1038/ng.f.136 · Cited by 1,131

Mining alleles for tar spot complex resistance from CIMMYT's maize Germplasm Bank

Willcox, M. C., Burgueño, J. A., Jeffers, D., Rodriguez-Chanona, E., Espinoza, A. G., Kehel, Z., Chepetla, D., Shrestha, R., Swarts, K., Buckler, E. S., et al. (2022) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2022.937200 · Cited by 5

Trans-Ethnic Fine-Mapping of Rare Causal Variants

Wang, X., & Teo, Y. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2824-8_18 · Cited by 5

Cohen’s h for detection of disease association with rare genetic variants

Wen, S., & Yeh, J. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-875 · Cited by 7

Genetic Architecture of Complex Human Traits: What Have We Learned from Genome-Wide Association Studies?

Zhang, G. (2015) · Current Genetic Medicine Reports · doi:10.1007/s40142-015-0083-9 · Cited by 5

Pathogenesis of type 1 diabetes: genetics

Pugliese, A. (2010) · Cited by 5

Lessons from the Genome-Wide Association Studies for Complex Multifactorial Disorders and Traits

Beckmann, J. S., & Antonarakis, S. E. (2009) · Springer eBooks · doi:10.1007/978-3-540-37654-5_10 · Cited by 5

A general statistic to test an optimally weighted combination of common and/or rare variants

Zhang, J., Wu, B., Sha, Q., Zhang, S., & Wang, X. (2019) · Genetic Epidemiology · doi:10.1002/gepi.22255 · Cited by 5

Bayesian model comparison for rare variant association studiesPreprint

Venkataraman, G. R., DeBoever, C., Tanigawa, Y., Aguirre, M., Ioannidis, A. G., Mostafavi, H., Spencer, C. C. A., Poterba, T., Bustamante, C. D., Daly, M. J., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/257162 · Cited by 5

PKR and the Integrated Stress Response drive immunopathology caused by ADAR1 mutationPreprint

Maurano, M. M., Snyder, J. M., Connelly, C. F., Henao‐Mejia, J., Sidrauski, C., & Stetson, D. B. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.30.405498 · Cited by 5

Exploring Random Forest in Genetic Risk Score Construction

Venkat, V., Clark, K., Jeng, X. J., Yao, T., Tsai, H., Lu, T., Hsiao, T., Lin, C., Holloway, S. T., Hoyo, C., et al. (2025) · Genetic Epidemiology · doi:10.1002/gepi.70022 · Cited by 4

Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer’s Disease

Jin, S. C., Benítez, B. A., Deming, Y. K., & Cruchaga, C. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2627-5_18 · Cited by 4

Secondary Analysis of Publicly Available Data Reveals Superoxide and Oxygen Radical Pathways are Enriched for Associations Between Type 2 Diabetes and Low‐Frequency Variants

Yazdanpanah, M., Chen, C., & Graham, J. (2013) · Annals of Human Genetics · doi:10.1111/ahg.12035 · Cited by 4

Using Gene Genealogies to Detect Rare Variants Associated with Complex Traits

Burkett, K. M., McNeney, B., Graham, J., & Greenwood, C. M. T. (2014) · Human Heredity · doi:10.1159/000363443 · Cited by 4

A Novel Genome-Information Content-Based Statistic for Genome-Wide Association Analysis Designed for Next-Generation Sequencing Data

Luo, L., Zhu, Y., & Xiong, M. (2012) · Journal of Computational Biology · doi:10.1089/cmb.2012.0035 · Cited by 3

Nonlinear dimension reduction with Wright–Fisher kernel for genotype aggregation and association mapping

Zhu, H., Li, L., & Zhou, H. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts406 · Cited by 4

Genetic Basis of Kidney Disease

Freedman, B. I., Bowden, D. W., & Rich, S. S. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4160-6193-9.10042-9 · Cited by 4

Isotype Defects

van der Burg, M., Weemaes, C. M. R., & Cunningham‐Rundles, C. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00016-9 · Cited by 4

Is the Association of the Rare rs35667974 IFIH1 Gene Polymorphism With Autoimmune Diseases a Case of RNA Epigenetics?

Andreou, A., Papakyriakou, A., Zervou, M. I., Goulielmos, G. N., & Eliopoulos, E. (2023) · Journal of Molecular Evolution · doi:10.1007/s00239-022-10090-0 · Cited by 4

Viruses and Autoimmune Diabetes in Rats

Mordes, J. P., Zipris, D., Liu, Z., & Blankenhorn, E. P. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4051-2_7 · Cited by 4

An insight into the genetics of type 1 Diabetes

Espino-Paisán, L., Urcelay, E., & Santiago, J. L. (2009) · Inmunología · doi:10.1016/s0213-9626(09)70040-x · Cited by 4

SNP discovery and evaluation with whole genome re-sequencing using pooled DNA in Japanese Black cattle

Hirano, T., Nishimura, S., Watanabe, T., Takasuga, A., HANZAWA, K., & Sugimoto, Y. (2013) · Nihon Chikusan Gakkaiho · doi:10.2508/chikusan.84.319 · Cited by 4

Enterovirus Neutralizing Antibodies, Monocyte Toll Like Receptors Expression and Interleukin Profiles Are Similar Between Non-affected and Affected Siblings From Long-Term Discordant Type 1 Diabetes Multiplex-Sib Families: The Importance of HLA Background

Bergamin, C. S., Hurtado, E. C. P., Oliveira, L. M. D. S., Gabbay, M. A. L., Piveta, V. M., Bittencourt, C., Russo, D. H., Carmona, R., Sato, M. N., & Dib, S. A. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.555685 · Cited by 4

The story of DNase II: A stifled death‐wish leads to self‐harm

Crow, Y. J. (2010) · European Journal of Immunology · doi:10.1002/eji.201040829 · Cited by 4

A Novel Support Vector Machine-Based Approach for Rare Variant Detection

Fang, Y., & Chiu, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071114 · Cited by 4

Polymorphisms in the interferon‐induced helicase ( IFIH 1) locus and susceptibility to A ddison's disease

Żurawek, M., Fichna, M., Januszkiewicz, D., Fichna, P., & Nowak, J. (2012) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2012.04497.x · Cited by 4

IRF-7: an Antiviral Factor and Beyond

Perrotti, E., Marsili, G., Sgarbanti, M., Remoli, A. L., Fragale, A., Acchioni, C., Orsatti, R., & Battistini, A. (2013) · Future Virology · doi:10.2217/fvl.13.88 · Cited by 4

Novel Insights Into the Etiology of Diabetes From Genome-Wide Association Studies

Palmer, C. N. A. (2009) · Diabetes · doi:10.2337/db09-1153 · Cited by 4

Plaque Psoriasis: Understanding Risk Factors of This Inflammatory Skin Pathology

Bélanger, A., de Oliveira, C. P., Maheux, M., & Pouliot, R. (2016) · Journal of Cosmetics Dermatological Sciences and Applications · doi:10.4236/jcdsa.2016.62009 · Cited by 4

A tree‐based gene–environment interaction analysis with rare features

Liu, M., Zhang, Q., & Ma, S. (2022) · Statistical Analysis and Data Mining The ASA Data Science Journal · doi:10.1002/sam.11578 · Cited by 4

Epidemiology and Pathogenesis of Type 1 Diabetes

Stene, L. C., & Lernmark, Å. (2023) · Springer eBooks · doi:10.1007/978-3-031-20999-4_2 · Cited by 3

MDA5 variants trade antiviral activity for protection from autoimmune disease

Wallace, C., Singh, R., & Modis, Y. (2025) · BMC Medical Genomics · doi:10.1186/s12920-025-02171-y · Cited by 4

Echovirus Epidemics, Autoimmunity, and Type 1 Diabetes

Díaz-Horta, O., Sarmiento, L., Baj, A., Cabrera‐Rode, E., & Toniolo, A. (2011) · InTech eBooks · doi:10.5772/22167 · Cited by 2

Statistical tests for detecting associations with groups of genetic variants: generalization, evaluation, and implementation

Ferguson, J. P., Wheeler, W., Fu, Y., Prokunina‐Olsson, L., Zhao, H., & Sampson, J. N. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.220 · Cited by 3

Rodent Models for Investigating the Dysregulation of Immune Responses in Type 1 Diabetes

Chou, F., Chen, H.-Y., Chen, S., Fang, M.-C., & Sytwu, H. (2013) · Journal of Diabetes Research · doi:10.1155/2013/138412 · Cited by 3

Epigenomic Factors in Human Obesity

Bell, C. G. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-388415-2.00014-7 · Cited by 3

Variant Identification in BARD1 , PRDM9 , RCC1 , and RECQL in Patients with Ovarian Cancer by Targeted Next-generation Sequencing of DNA Pools

Suszyńska, M., Ratajska, M., Galka-Marciniak, P., Ryszkowska, A., Wydra, D. G., Debniak, J., Jasiak, A., Wasąg, B., Cybulski, C., & Kozlowski, P. (2021) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-21-0295 · Cited by 3

Case-only exome variation analysis of severe alcohol dependence using a multivariate hierarchical gene clustering approach

Gentry, A. E., Alexander, J. C., Ahangari, M. M., Peterson, R. E., Miles, M. F., Bettinger, J. C., Davies, A. G., Groteweil, M., Bacanu, S., Kendler, K. S., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0283985 · Cited by 2

Genetic Variation in the CYP2C Monooxygenase Enzyme Subfamily Shows No Association With Longevity in a German Population

Flachsbart, F., Ufer, M., Kleindorp, R., Nikolaus, S., Schreiber, S., & Nebel, A. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr117 · Cited by 3

Role of Genetic Factors in Pathophysiology of Multiple Sclerosis

Goris, A., Dubois, B., & Hilven, K. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800763-1.00008-7 · Cited by 3

A modified association test for rare and common variants based on affected sib-pair design

Guo, Y., & Zhou, Y. (2019) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2019.01.014 · Cited by 3

Fremskritt innen diabetesgenetikk

Njølstad, P. R., Hertel, J. K., Sövik, O., Ræder, H., Johansson, S., & Molven, A. (2010) · Tidsskrift for Den norske legeforening · doi:10.4045/tidsskr.09.1035 · Cited by 3

NHLBI clinical trials workshop: an executive summary

Zheng, G., Wu, C. O., Yang, S., Waclawiw, M. A., DeMets, D. L., & Geller, N. L. (2012) · Statistics in Medicine · doi:10.1002/sim.5406 · Cited by 3

Association analysis of whole genome sequencing data accounting for longitudinal and family designs

Hu, Y., Hui, Q., & Sun, Y. V. (2014) · BMC Proceedings · doi:10.1186/1753-6561-8-s1-s89 · Cited by 4

A statistical method for scanning the genome for regions with rare disease alleles

Garner, C. P. (2010) · Genetic Epidemiology · doi:10.1002/gepi.20483 · Cited by 3

Type 1 diabetes research: Newer approaches and exciting developments

Sanjeevi, C. (2009) · International Journal of Diabetes in Developing Countries · doi:10.4103/0973-3930.53119 · Cited by 3

Statistical Selection Strategy for Risk and Protective Rare Variants Associated with Complex Traits

Kim, S., Lee, K., & Sun, H. (2015) · Journal of Computational Biology · doi:10.1089/cmb.2015.0091 · Cited by 3

Research strategies for the next step of genome-wide association study

Quan, C., & ZHANG, X.-J. (2011) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2011.00100 · Cited by 3

Understanding the Pathogenesis of Endometriosis: Gene Mapping Studies

Painter, J. N., Zondervan, K. T., & Montgomery, G. W. (2011) · Wiley eBooks · doi:10.1002/9781444398519.ch6 · Cited by 3

A study on the role of genes of innate immunity in type 1 diabetes

Sedimbi, S. K. (2010) · Figshare · Cited by 3

The accelerator hypothesis: insulin resistance as the central cause of type 1 and type 2 diabetes

Booker, C. S. (2009) · International Journal of Obesity · doi:10.1038/ijo.2009.190 · Cited by 3

RIG ‐ I ‐Like Receptors

Yong, H. Y., & Luo, D. (2015) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0026237 · Cited by 3

PADI3 , hair disorders and genomic investigation

McGrath, J. A., Ohyama, M., & Simpson, M. A. (2019) · British Journal of Dermatology · doi:10.1111/bjd.18463 · Cited by 3

Unraveling the immune activation mechanisms of DAMPs in coronary artery disease through transcriptomic and single-cell analyses

Li, Y., Shi, H., Zou, Y., Guan, Y., Liu, N., & Liu, B. (2025) · Cytokine · doi:10.1016/j.cyto.2025.156952 · Cited by 2

Gene variants of interferon induced with helicase C domain 1 in Japanese patients with Dermatomyositis-associated rapidly progressive interstitial lung disease: a genetic association study using whole-exome and Sanger sequencing

Okamoto, M., Yoshida, A., Zaizen, Y., Ishida, M., Shimizu, T., Sakamoto, N., Hozumi, H., Yamano, Y., Gono, T., Matsuo, N., et al. (2025) · Respiratory Research · doi:10.1186/s12931-025-03379-3 · Cited by 2

A cytoplasmic index for quantifying immune-related A-to-I RNA editing

Cohen‐Fultheim, R., Twersky, I., Krupkin, H., Roth, S. H., Levanon, E. Y., & Eisenberg, E. (2026) · Genome biology · doi:10.1186/s13059-026-04154-3 · Cited by 2

Diabetes: A comprehensive review of the Indian landscape in contrast with global trends

Rana, N. S., Vishvakarma, N. K., Sonkar, S. C., & Beg, M. M. A. (2026) · World Journal of Diabetes · doi:10.4239/wjd.v17.i2.110701 · Cited by 3

Mapping the gene regulatory landscape of archaic hominin introgression in modern Papuans

Comerford, M., Vespasiani, D. M., Shukla, N., Cook, L. E., Yermakovich, D., Dannemann, M., Leavesley, M., Kinipi, C., Ricaut, F., Brucato, N., et al. (2026) · PLoS Genetics · doi:10.1371/journal.pgen.1012067 · Cited by 2

A Powerful Approach to Test an Optimally Weighted Combination of Rare Variants in Admixed Populations

Wang, X., Zhang, S., Li, Y., Li, M., & Sha, Q. (2015) · Genetic Epidemiology · doi:10.1002/gepi.21894 · Cited by 3

On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium

Lipman, P. J., Yip, W., AlChawa, T., Ludwig, K. U., Mangold, E., & Lange, C. (2011) · Genetic Epidemiology · doi:10.1002/gepi.20638 · Cited by 2

Poisson Approximation–Based Score Test for Detecting Association of Rare Variants

Fang, H., Zhang, H., & Yang, Y. (2016) · Annals of Human Genetics · doi:10.1111/ahg.12154 · Cited by 3

Genetic markers for psoriatic arthritis in patients with psoriasis. Part I: non-HLA genes

Kubanov, A. A., Karamova, A. Е., Chikin, V. V., Анатольевич, В. Д., Znamenskaya, L. F., & Artamonova, O. G. (2021) · Vestnik dermatologii i venerologii · doi:10.25208/vdv1260 · Cited by 2

A Targeted Deep Sequencing Method to Quantify Endogenous Retrovirus Gag Sequence Variants and Open Reading Frames Expressed in Nonobese Diabetic Mice

Dai, Y. D., Du, W., Wang, Y., & Hu, W.-Y. (2024) · The Journal of Immunology · doi:10.4049/jimmunol.2300660 · Cited by 2

Interferons in human inborn errors of disease

Stine, L., Cahill, S. E., & Humphries, F. (2025) · mBio · doi:10.1128/mbio.01570-25 · Cited by 2

Protective association exhibited by a single nucleotide polymorphism of the IFIH1 gene in patients with psoriasis: A case-control study

Luna, E. V. E., Sierra, C. J. E., Cornejo-Sanchez, D. M., Sanclemente, G., & Pineda-Trujillo, N. (2021) · Medwave · doi:10.5867/medwave.2021.11.002099 · Cited by 2

An Evolutionary Biology Approach to Understanding Neurological Disorders

Aziz, A., Ilievska, J., Paul, R., & Naomi, E. (2012) · InTech eBooks · doi:10.5772/37919 · Cited by 2

Population Genetics and Pharmacogenetics

Ong, K. K., & Elks, C. E. (2010) · Yearbook of pediatric endocrinology · doi:10.1159/000320661 · Cited by 2

Rare variants analysis by risk-based variable-threshold method

Fang, H., Hou, B., Wang, Q., & Yang, Y. (2013) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2013.04.001 · Cited by 3

A weighted accumulation test for associating rare genetic variation with quantitative phenotypes

Xing, C., Satten, G. A., & Allen, A. S. (2011) · BMC Proceedings · doi:10.1186/1753-6561-5-s9-s6 · Cited by 2

Novel tree-based method to generate markers from rare variant data

Jiang, Y., Brennan, J. S., Calixte, R., He, Y., Nyirabahizi, E., & Heping Zhang, D. (2011) · BMC Proceedings · doi:10.1186/1753-6561-5-s9-s102 · Cited by 2

Genome-wide association studies and genetic architecture of common human diseases

Montgomery, G. W. (2011) · BMC Proceedings · doi:10.1186/1753-6561-5-s4-s16 · Cited by 2

Power of Rare Variant Aggregate Tests

Rivas, M. A., & Moutsianas, L. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2824-8_13 · Cited by 2

Longitudinal data analysis for rare variants detection with penalized quadratic inference function

Cao, H., Li, Z., Yang, H., Cui, Y., & Zhang, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-00712-9 · Cited by 2

Detecting Multiethnic Rare Variants

Ouyang, W., Zhu, X., & Qin, H. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7274-6_26 · Cited by 2

Prediabetes Induced by a Single Autoimmune B Cell Clone

Phillips, N., Ke, E., Nham, A., Seidl, M., Freeman, B., Abadejos, J. R., Xiao, C., Nemazee, D. A., Ku, M., & Kirak, O. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01073 · Cited by 2

Genetics of type 1 diabetes mellitus

Savage, D. A., & Bain, S. C. (2011) · doi:10.1093/med/9780199235292.003.1316 · Cited by 2

Pathogenesis of Type 1 Diabetes

Pugliese, A. (2018) · Endocrinology · doi:10.1007/978-3-319-45015-5_7 · Cited by 2

Genetic Basis of Intervertebral Disc Degeneration

Yee, A., & Chan, D. T.-M. (2013) · Springer eBooks · doi:10.1007/978-3-7091-1535-0_10 · Cited by 3

Unravelling the Proteomics of HLA-B*57:01+ Antigen Presenting Cells during Abacavir Medication

Haukamp, F. J., Gall, E., Hò, G. T., Hiemisch, W., Stieglitz, F., Kühn, J., Blasczyk, R., Pich, A., & Bade‐Doeding, C. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12010040 · Cited by 2

Molecular Genetics of Endometriosis

Painter, J. N., Zondervan, K. T., Missmer, S. A., & Montgomery, G. W. (2011) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0021473 · Cited by 2

Analysis of Gene–Gene Interactions Underlying Human Disease

Wen, Y., & Lu, Q. L. (2014) · Wiley eBooks · doi:10.1002/9780470015902.a0022498 · Cited by 3

The Molecular Genetics of Type 2 Diabetes: Past, Present and Future

Tan, J. T., Chia, K. S., & Ku, C. (2009) · Wiley eBooks · doi:10.1002/9780470015902.a0021994 · Cited by 2

Genetics of Graves' Disease

Hamilton, A., Gough, S. C. L., & Simmonds, M. J. (2013) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0024977 · Cited by 2

Studies of Immune Regulation in Type 1 Diabetes

Honkanen, J. K. (2010) · Työväentutkimus Vuosikirja · Cited by 2

After the Gwas rush: Nuggets of insight into the pathogenesis of autoimmune disease

Danska, J. S., & Poussier, P. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.10.007 · Cited by 2

Genome-wide association studies: providers of candidate genes for identification of rare variants?

Barc, J., & Koopmann, T. T. (2011) · EP Europace · doi:10.1093/europace/eur050 · Cited by 2

Evidence of population specific selection inferred from 289 genome sequences of Nilo-Saharan and Niger-Congo linguistic groups in AfricaPreprint

Mulindwa, J., Noyes, H. A., Ilboudo, H., Nyangiri, O. A., Koffi, M., Ngoyi, D. M., Simo, G., Enyaru, J., Chisi, J., Simuunza, M. C., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/186700 · Cited by 2

Rotavirus and Type 1 Diabetes

Honeyman, M. C., & Harrison, L. C. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4051-2_18 · Cited by 1

Type 1 Diabetes Mellitus

Chen, W., Xie, A., Wu, J., & Chan, L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800563-7.00007-5 · Cited by 1

Extra X, extra questions: Trisomy X syndrome and IgA deficiency – a case report

Leone, F., Gori, A., Cinicola, B. L., Brindisi, G., Maglione, V., Anania, C., & Zicari, A. M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1518076 · Cited by 1

Interplay between the host genome, autoimmune disease and infection

Martin, M., Sanchiz, Á., & Navasa, N. (2025) · Advances in genetics · doi:10.1016/bs.adgen.2025.02.006 · Cited by 1

Speculation on Prevention of Type 1 Diabetes

Insel, R. (2013) · Springer eBooks · doi:10.1007/978-1-4614-4051-2_31 · Cited by 1

Neuroblastoma and Whole Genome Searches

Capasso, M. (2012) · InTech eBooks · doi:10.5772/34582 · Cited by 1

The Genetics of Type 1 Diabetes

Kathleen, M. (2011) · InTech eBooks · doi:10.5772/21924 · Cited by 1

Islet Endothelium: Role in Type 1 Diabetes and in Coxsackievirus Infections

Favaro, E., Miceli, I., Camussi, E., & Maria, M. (2011) · InTech eBooks · doi:10.5772/24389 · Cited by 1

Approaches for Dissection of the Genetic Basis of Complex Disease Development in Human

Nicole, J., Bozaoglu, K., Abdul, W., & Jowett, J. B. M. (2012) · InTech eBooks · doi:10.5772/35074 · Cited by 1

Use of RNA Domains in the Viral Genome as Innate Immunity Inducers for Antiviral Strategies and Vaccine Improvement

Rodríguez‐Pulido, M., Sobrino, F., Borrego, B., & S�iz, M. (2013) · InTech eBooks · doi:10.5772/56099 · Cited by 1

Evaluating the Coverage and Potential of Imputing the Exome Microarray with Next-Generation Imputation Using the 1000 Genomes Project

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