PON-P: Integrated predictor for pathogenicity of missense variants von Olatubosun, Ayodeji, Väliaho, Jouni, Härkönen, Jani, Thusberg, Janita, Vihinen, Mauno

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Immunodeficiency mutation databases (IDbases) von Piirilä, Hilkka, Väliaho, Jouni, Vihinen, Mauno

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BTKbase: the mutation database for X-linked agammaglobulinemia von Väliaho, Jouni, Smith, C.I. Edvard, Vihinen, Mauno

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Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling von Lindvall, Jessica M., Blomberg, K. Emelie M., Väliaho, Jouni, Vargas, Leonardo, Heinonen, Juhana E., Berglöf, Anna, Mohamed, Abdalla J., Nore, Beston F., Vihinen, Mauno, Smith, C. I. Edvard

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Structure-function analysis indicates that sumoylation modulates DNA-binding activity of STAT1 von Grönholm, Juha, Vanhatupa, Sari, Ungureanu, Daniela, Väliaho, Jouni, Laitinen, Tuomo, Valjakka, Jarkko, Silvennoinen, Olli

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Immunodeficiency mutation databases (IDbases) von Piirilä, Hilkka, Väliaho, Jouni, Vihinen, Mauno

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Characterization of All Possible Single-Nucleotide Change Caused Amino Acid Substitutions in the Kinase Domain of Bruton Tyrosine Kinase von Väliaho, Jouni, Faisal, Imrul, Ortutay, Csaba, Smith, C. I. Edvard, Vihinen, Mauno

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IDR knowledge base for primary immunodeficiencies von Samarghitean, Crina, Väliaho, Jouni, Vihinen, Mauno

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BTKbase, Bruton Tyrosine Kinase Variant Database in X-Linked Agammaglobulinemia: Looking Back and Ahead von Schaafsma, Gerard C. P., Väliaho, Jouni, Wang, Qing, Berglöf, Anna, Zain, Rula, Smith, C. I. Edvard, Vihinen, Mauno

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Assessing computational predictions of the phenotypic effect of cystathionine‐beta‐synthase variants von Kasak, Laura, Bakolitsa, Constantina, Hu, Zhiqiang, Yu, Changhua, Rine, Jasper, Dimster‐Denk, Dago F., Pandey, Gaurav, Baets, Greet, Bromberg, Yana, Cao, Chen, Capriotti, Emidio, Casadio, Rita, Durme, Joost, Giollo, Manuel, Karchin, Rachel, Katsonis, Panagiotis, Leonardi, Emanuela, Lichtarge, Olivier, Martelli, Pier Luigi, Masica, David, Mooney, Sean D., Olatubosun, Ayodeji, Radivojac, Predrag, Rousseau, Frederic, Pal, Lipika R., Savojardo, Castrense, Schymkowitz, Joost, Thusberg, Janita, Tosatto, Silvio C.E., Vihinen, Mauno, Väliaho, Jouni, Repo, Susanna, Moult, John, Brenner, Steven E., Friedberg, Iddo

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Distribution of immunodeficiency fact files with XML--from Web to WAP von Väliaho, Jouni, Riikonen, Pentti, Vihinen, Mauno

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PhenCode: connecting ENCODE data with mutations and phenotype von Giardine, Belinda, Riemer, Cathy, Hefferon, Tim, Thomas, Daryl, Hsu, Fan, Zielenski, Julian, Sang, Yunhua, Elnitski, Laura, Cutting, Garry, Trumbower, Heather, Kern, Andrew, Kuhn, Robert, Patrinos, George P., Hughes, Jim, Higgs, Doug, Chui, David, Scriver, Charles, Phommarinh, Manyphong, Patnaik, Santosh K., Blumenfeld, Olga, Gottlieb, Bruce, Vihinen, Mauno, Väliaho, Jouni, Kent, Jim, Miller, Webb, Hardison, Ross C.

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IDR: the ImmunoDeficiency Resource von Väliaho, Jouni, Pusa, Marianne, Ylinen, Tuomo, Vihinen, Mauno

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Structural basis of Bloom syndrome (BS) causing mutations in the BLM helicase domain von Rong, S B, Väliaho, J, Vihinen, M

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KinMutBase: A registry of disease-causing mutations in protein kinase domains von Ortutay, Csaba, Väliaho, Jouni, Stenberg, Kaj, Vihinen, Mauno

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V(D)J recombination defects in lymphocytes due to RAG mutations : severe immunodeficiency with a spectrum of clinical presentations von VILLA, Anna, SOBACCHI, Cristina, CORTES, Patricia, DUSE, Marzia, FASTH, Anders, FILIPOVICH, Alexandra M, INFANTE, Anthony J, JONES, Alison, MAZZOLARI, Evelina, MULLER, Susanna M, PASIC, Srdjan, RECHAVI, Gideon, NOTARANGELO, Luigi D, SACCO, Maria Grazia, SANTAGATA, Sandro, SCHROEDER, Marlis L, SEGER, Reinhard, STRINA, Dario, UGAZIO, Alberto, VÄLIAHO, Jouni, VIHINEN, Mauno, VOGLER, Larry B, OCHS, Hans, BOZZI, Fabio, VEZZONI, Paolo, FRIEDRICH, Wilhelm, SCHWARZ, Klaus, ABINUN, Mario, ABRAHAMSEN, Tore G, ARKWRIGHT, Peter D, BANIYASH, Michal, BROOKS, Edward G, CONLEY, Mary Ellen

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BDTKbase:: The mutation database for X-linked agammaglobullinemia von Valiaho, J, Smith, CIE, Vihinen, M

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KinMutBase: A registry of disease-causing mutations in protein kinase domains: KinMutBase von Ortutay, Csaba, Väliaho, Jouni, Stenberg, Kaj, Vihinen, Mauno

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Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia von Vihinen, Mauno, Kwan, Sau-Ping, Lester, Tracy, Ochs, Hans D., Resnick, Igor, Väliaho, Jouni, Conley, Mary Ellen, Smith, C.I. Edvard

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Online registry of genetic and clinical immunodeficiency diagnostic laboratories, IDdiagnostics von Samarghitean, Crina, Väliaho, Jouni, Vihinen, Mauno

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