Kere, Juha

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Collaborative Association Study of Psoriasis (CASP), Tsoi, L. C., Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2, Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., et al. (2012) · Nature Genetics

Psoriasis: Treatment and PathogenesisGenetic Associations and Epidemiology

Cited by 1,024

DNA methylation in newborns and maternal smoking in pregnancy: genome-wide consortium meta-analysis

Joubert, B. R., Felix, J. F., Yousefi, P., Bakulski, K. M., Just, A. C., Breton, C., Reese, S. E., Markunas, C. A., Richmond, R. C., Xu, C.-J., et al. (2016) · The American Journal of Human Genetics

Epigenetics and DNA MethylationBirth, Development, and Health

Cited by 886

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Kere, J., Srivastava, A. K., Montonen, O., Zonana, J., Thomas, N., Ferguson, B., Munoz, F., Morgan, D., Clarke, A., Baybayan, P., et al. (1996) · Nature Genetics

dental development and anomaliesHair Growth and Disorders

Cited by 749

Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus

Lee-Kirsch, M. A., Gong, M., Chowdhury, D., Senenko, L., Engel, K., Lee, Y.-A., de Silva, U., Bailey, S. L., Witte, T., Vyse, T. J., et al. (2007) · Nature Genetics

Systemic Lupus Erythematosus ResearchSystemic Sclerosis and Related Diseases

Cited by 730

Drug repositioning: a machine-learning approach through data integration

Napolitano, F., Zhao, Y., Moreira, V. M., Tagliaferri, R., Kere, J., D’Amato, M., & Greco, D. (2013) · Journal of Cheminformatics

Computational Drug Discovery MethodsBioinformatics and Genomic Networks

Cited by 349

FANTOM5 CAGE profiles of human and mouse samples

Noguchi, S., Arakawa, T., Fukuda, S., Furuno, M., Hasegawa, A., Hori, F., Ishikawa-Kato, S., Kaida, K., Kaiho, A., Kanamori-Katayama, M., et al. (2017) · Scientific Data

Genomics and Chromatin DynamicsGenomics and Phylogenetic Studies

Cited by 310

Epigenome-Wide Meta-Analysis of Methylation in Children Related to Prenatal NO2 Air Pollution Exposure

Gruzieva, O., Xu, C.-J., Breton, C. V., Annesi-Maesano, I., Antó, J. M., Auffray, C., Ballereau, S., Bellander, T., Bousquet, J., Bustamante, M., et al. (2017) · Environmental Health Perspectives

Epigenetics and DNA MethylationAir Quality and Health Impacts

Cited by 227

Human pluripotent reprogramming with CRISPR activators

Weltner, J., Balboa, D., Katayama, S., Bespalov, M., Krjutškov, K., Jouhilahti, E.-M., Trokovic, R., Kere, J., & Otonkoski, T. (2018) · Nature Communications

Pluripotent Stem Cells ResearchCRISPR and Genetic Engineering

Cited by 181

Influence of the COMT genotype on working memory and brain activity changes during development

Dumontheil, I., Roggeman, C., Ziermans, T., Peyrard-Janvid, M., Matsson, H., Kere, J., & Klingberg, T. (2011) · Biological Psychiatry

Neurotransmitter Receptor Influence on BehaviorCognitive Abilities and Testing

Cited by 165

Timing of infant feeding in relation to childhood asthma and allergic diseases

Nwaru, B. I., Takkinen, H.-M., Niemelä, O., Kaila, M., Erkkola, M., Ahonen, S., Haapala, A.-M., Kenward, M. G., Pekkanen, J., Lahesmaa, R., et al. (2013) · Journal of Allergy and Clinical Immunology

Asthma and respiratory diseasesFood Allergy and Anaphylaxis Research

Cited by 151

Identification of a basolateral Cl−/HCO 3 − exchanger specific to gastric parietal cells

Petrovic, S., Ju, X., Barone, S., Seidler, U., Alper, S. L., Lohi, H., Kere, J., & Soleimani, M. (2003) · American Journal of Physiology-Gastrointestinal and Liver Physiology

Ion Transport and Channel RegulationATP Synthase and ATPases Research

Cited by 91

The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia: Mutations in Brief

Pääkkönen, K., Cambiaghi, S., Novelli, G., Ouzts, L. V., Penttinen, M., Kere, J., & Srivastava, A. K. (2001) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 73

The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

Bölte, S., Willfors, C., Berggren, S., Norberg, J., Poltrago, L., Mevel, K., Coco, C., Fransson, P., Borg, J., Sitnikov, R., et al. (2014) · Twin Research and Human Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 71

The CCHCR1 (HCR) gene is relevant for skin steroidogenesis and downregulated in cultured psoriatic keratinocytes

Tiala, I., Suomela, S., Huuhtanen, J., Wakkinen, J., Hölttä-Vuori, M., Kainu, K., Ranta, S., Turpeinen, U., Hämäläinen, E., Jiao, H., et al. (2007) · Journal of Molecular Medicine

Psoriasis: Treatment and PathogenesisDermatology and Skin Diseases

Cited by 64

The diagnosis of pre-eclampsia using two revised classifications in the Finnish Pre-eclampsia Consortium (FINNPEC) cohort

Kallela, J., Jääskeläinen, T., Kortelainen, E., Heinonen, S., Kajantie, E., Kere, J., Kivinen, K., Pouta, A., & Laivuori, H. (2016) · BMC Pregnancy and Childbirth

Pregnancy and preeclampsia studiesNeurological Complications and Syndromes

Cited by 48

Primary cilia promote the differentiation of human neurons through the WNT signaling pathway

Coschiera, A., Yoshihara, M., Lauter, G., Ezer, S., Pucci, M., Li, H., Kavšek, A., Riedel, C. G., Kere, J., & Swoboda, P. (2024) · BMC Biology

Genetic and Kidney Cyst DiseasesNeurogenesis and neuroplasticity mechanisms

Cited by 26