Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals by Ågren, Richard, Patil, Snehal, Zhou, Xiang, Sahlholm, Kristoffer, Pääbo, Svante, Zeberg, Hugo

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Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency by Heeney, Matthew M., Guo, Dongjing, De Falco, Luigia, Campagna, Dean R., Olbina, Gordana, Kao, Paige P.-C., Schmitz-Abe, Klaus, Rahimov, Fedik, Gutschow, Patrick, Westerman, Keith, Ostland, Vaughn, Jackson, Tracy, Klaassen, Robert J., Markianos, Kyriacos, Finberg, Karin E., Iolascon, Achille, Westerman, Mark, London, Wendy B., Fleming, Mark D.

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An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects by Fakhouri, Walid D., Rahimov, Fedik, Attanasio, Catia, Kouwenhoven, Evelyn N., Ferreira De Lima, Renata L., Felix, Temis Maria, Nitschke, Larissa, Huver, David, Barrons, Julie, Kousa, Youssef A., Leslie, Elizabeth, Pennacchio, Len A., Van Bokhoven, Hans, Visel, Axel, Zhou, Huiqing, Murray, Jeffrey C., Schutte, Brian C.

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Human skeletal muscle xenograft as a new preclinical model for muscle disorders by Zhang, Yuanfan, King, Oliver D, Rahimov, Fedik, Jones, Takako I, Ward, Christopher W, Kerr, Jaclyn P, Liu, Naili, Emerson, Jr, Charles P, Kunkel, Louis M, Partridge, Terence A, Wagner, Kathryn R

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Variation in the HLA-G Promoter Region Influences Miscarriage Rates by Ober, Carole, Aldrich, Carrie L., Chervoneva, Inna, Billstrand, Christine, Rahimov, Fedik, Gray, Heather L., Hyslop, Terry

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Functional characterization of a single nucleotide polymorphism associated with Alzheimer's disease in a hiPSC-based neuron model by Lindsay R Stolzenburg, Sahar Esmaeeli, Ameya S Kulkarni, Erin Murphy, Taekyung Kwon, Christina Preiss, Lamiaa Bahnassawy, Joshua D Stender, Justine D Manos, Peter Reinhardt, Fedik Rahimov, Jeffrey F Waring, Cyril Y Ramathal

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A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function by HOMMA, Sachiko, CHEN, Jennifer Cj, RAHIMOV, Fedik, BEERMANN, Mary Lou, HANGER, Kendal, BIBAT, Genila M, WAGNER, Kathryn R, KUNKEL, Louis M, EMERSON, Charles P, BOONE MILLER, Jeffrey

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The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections by Maisha, Fahrisa I., Strausz, Satu J., Lammi, Vilma, Plenge, Robert, Ehm, Margaret G., Auro, Kirsi, Longerich, Simonne, Chatelain, Clement, O´Donnell, Chris, Kaprio, Jaakko, Virolainen, Petri, Raivio, Taneli, Tikkanen, Jani, Kosma, Veli-Matti, Laukkanen, Jari, Ding, Zhihao, Hu, Xinli, Hedman, Åsa, Renaud, Nicole, Ripatti, Samuli, Arvas, Mikko, Hinttala, Reetta, Kettunen, Johannes, Mäkelä, Johanna, Hiltunen, Mikko, Peltola, Jukka, Raivio, Minna, Partanen, Juulia, Abbasi, Ali, Eaton, Susan, Xu, Fanli, Addis, Laura, Eicher, John, Pikkarainen, Sampsa, Jussila, Airi, Voutilainen, Markku, Miller, Jason, Miller, Melissa, Eklund, Kari, Lertratanakul, Apinya, Pelkonen, Margit, Mouded, Majd, Ngo, Debby, Niiranen, Teemu, Aittokallio, Jenni, Hernesniemi, Jussi, Hiltunen, Timo, Reeve, Mary Pat, Mattson, Johanna, Auranen, Annika, Auvinen, Päivi, Fabre, Margarete, Kulkarni, Diptee, Loboda, Andrey, Ollila, Terhi, Loomis, Stephanie, Hannula-Jouppi, Katariina, Salmi, Teea, Pussinen, Pirkko, Salo, Tuula, Siponen, Maria, Mäntylä, Päivi, Anttonen, Vuokko, Kotaniemi-Talonen, Laura, Välimäki, Niko, Laakkonen, Eija, Laisk, Triin, Isometsä, Erkki, Ollila, Hanna, Mäkitie, Antti, Aarnisalo, Antti, Aittomäki, Kristiina, Havulinna, Aki, Della Briotta Parolo, Pietro, Liu, Aoxing, Ganna, Andrea, Heyne, Henrike, Rodosthenous, Rodos, Palotie, Tuula, Palin, Kimmo, Garcia-Tabuenca, Javier, Siirtola, Harri, Kristiansson, Kati, Ritari, Jarmo, Pylkäs, Katri, Karjalainen, Minna, Mantere, Tuomo, Siltanen, Sanna, Kuopio, Teijo, Kajanne, Risto, Aavikko, Mervi, Zheng, Zhili, Kaunisto, Mari, Kytölä, Anastasia, Weldatsadik, Rigbe, Laiho, Päivi, Wong, Regis, Koskelainen, Sami, Lehto, Petri, Redline, Susan

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Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway by Jugessur, Astanand, Rahimov, Fedik, Lie, Rolv T., Wilcox, Allen J., Gjessing, Håkon K., Nilsen, Roy M., Nguyen, Truc Trung, Murray, Jeffrey C.

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Gene expression profiling of skeletal muscles treated with a soluble activin type IIB receptor by Rahimov, Fedik, King, Oliver D, Warsing, Leigh C, Powell, Rachel E, Emerson, Jr, Charles P, Kunkel, Louis M, Wagner, Kathryn R

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Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers by Rahimov, Fedik, King, Oliver D, Leung, Doris G, Bibat, Genila M, Emerson, Charles P, Kunkel, Louis M, Wagner, Kathryn R

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Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2 by Mitsuhashi, Satomi, Boyden, Steven E, Estrella, Elicia A, Jones, Takako I, Rahimov, Fedik, Yu, Timothy W, Darras, Basil T, Amato, Anthony A, Folkerth, Rebecca D, Jones, Peter L, Kunkel, Louis M, Kang, Peter B

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GL beta mutations in four Brazilian patients: How wide is the phenotypic spectrum? by Rahimov, Fedik, Ribeiro, Lucilene Arilho, de Miranda, Eziquiel, Richieri-Costa, Antonio, Murray, Jeffrey C

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Medical sequencing of candidate genes for nonsyndromic cleft lip and palate by Alexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, Ecaterina Dragan, Têmis M Félix, Fedik Rahimov, Jill Harrington, Rebecca R Schultz, Yoriko Watanabe, Marla Johnson, Jennifer Fang, Sarah E O'Brien, Iêda M Orioli, Eduardo E Castilla, David R Fitzpatrick, Rulang Jiang, Mary L Marazita, Jeffrey C Murray

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Direct Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate by Vieira, Alexandre Rezende, Avila, Joseph Ross, Daack-Hirsch, Sandra, Dragan, Ecaterina, Felix, Temis M., Rahimov, Fedik, Harrington, Jill, Schultz, Rebecca R., Watanabe, Yoriko, Johnson, Marla, Fang, Jennifer, O'Brien, Sarah E., Orioli, Ieda M., Castilla, Eduardo E., FitzPatrick, David R., Jiang, Rulang, Marazita, Mary L., Murray, Jeffrey C.

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