Another burden by Cappuccio, Ronald J

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Views of Our Readers by Kennedy, Robert H., Schoen, Edgar J., Stith, Richard, Weinroth, Lora S., Tribe, Laurence H., Kemper, Kurt, Cappuccio, Ronald J., Kaap, Keith J., Shuttleworth, Kenneth R., Hawkins, Robert G., Norby, Dennis W.

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature by Rots, Dmitrijs, Chater-Diehl, Eric, Dingemans, Alexander J.M., Goodman, Sarah J., Siu, Michelle T., Cytrynbaum, Cheryl, Choufani, Sanaa, Hoang, Ny, Walker, Susan, Awamleh, Zain, Charkow, Joshua, Meyn, Stephen, Pfundt, Rolph, Rinne, Tuula, Gardeitchik, Thatjana, de Vries, Bert B.A., Deden, A. Chantal, Leenders, Erika, Kwint, Michael, Stumpel, Constance T.R.M., Stevens, Servi J.C., Vermeulen, Jeroen R., van Harssel, Jeske V.T., Bosch, Danielle G.M., van Gassen, Koen L.I., van Binsbergen, Ellen, de Geus, Christa M., Brackel, Hein, Hempel, Maja, Lessel, Davor, Denecke, Jonas, Slavotinek, Anne, Strober, Jonathan, Crunk, Amy, Folk, Leandra, Wentzensen, Ingrid M., Yang, Hui, Zou, Fanggeng, Millan, Francisca, Person, Richard, Xie, Yili, Liu, Shuxi, Ousager, Lilian B., Larsen, Martin, Schultz-Rogers, Laura, Morava, Eva, Klee, Eric W., Berry, Ian R., Campbell, Jennifer, Lindstrom, Kristin, Pruniski, Brianna, Neumeyer, Ann M., Radley, Jessica A., Phornphutkul, Chanika, Schmidt, Berkley, Wilson, William G., Õunap, Katrin, Reinson, Karit, Pajusalu, Sander, van Haeringen, Arie, Ruivenkamp, Claudia, Cuperus, Roos, Santos-Simarro, Fernando, Palomares-Bralo, María, Pacio-Míguez, Marta, Ritter, Alyssa, Bhoj, Elizabeth, Tønne, Elin, Tveten, Kristian, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Rowe, Leah, Bunn, Jason, Saenz, Margarita, Platzer, Konrad, Mertens, Mareike, Caluseriu, Oana, Nowaczyk, Małgorzata J.M., Cohn, Ronald D., Kannu, Peter, Alkhunaizi, Ebba, Chitayat, David, Scherer, Stephen W., Brunner, Han G., Vissers, Lisenka E.L.M., Kleefstra, Tjitske, Koolen, David A., Weksberg, Rosanna

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Genetic variants linked to education predict longevity by Marioni, Riccardo E., Ritchie, Stuart J., Joshi, Peter K., Hagenaars, Saskia P., Okbay, Aysu, Fischer, Krista, Adams, Mark J., Hill, W. David, Davies, Gail, Nagy, Reka, Amador, Carmen, Läll, Kristi, Metspalu, Andres, Liewald, David C., Campbell, Archie, Wilson, James F., Hayward, Caroline, Esko, Tõnu, Porteous, David J., Gale, Catharine R., Deary, Ian J.

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Prevalence and Penetrance of HFE Mutations in 4865 Unselected Primary Care Patients by Phatak, Pradyumna D., Ryan, Daniel H., Cappuccio, Joseph, Oakes, David, Braggins, Caroline, Provenzano, Kim, Eberly, Shirley, Sham, Ronald L.

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Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles by Sham, Ronald L., Raubertas, Richard F., Braggins, Caroline, Cappuccio, Joseph, Gallagher, Margaret, Phatak, Pradyumna D.

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Correlation Between Genotype and Phenotype in Hereditary Hemochromatosis: Analysis of 61 Cases by Sham, Ronald L., Ou, Chin-Yih, Cappuccio, Joseph, Braggins, Caroline, Dunnigan, Karin, Phatak, Pradyumna D.

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Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles by Sham, Ronald L., Raubertas, Richard F., Braggins, Caroline, Cappuccio, Joseph, Gallagher, Margaret, Phatak, Pradyumna D.

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