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16,826 results

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Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, Moreno L, Arcos-Burgos M, Lidral AC, Field LL, Liu YE, Ray A, Goldstein TH, Schultz RE, Shi M, Johnson MK, Kondo S, Schutte BC, Marazita ML, Murray JC. Zucchero TM, et al. Among authors: suzuki y. N Engl J Med. 2004 Aug 19;351(8):769-80. doi: 10.1056/NEJMoa032909. N Engl J Med. 2004. PMID: 15317890 Free article.
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC. Butali A, et al. Among authors: suzuki y, suzuki s. Am J Med Genet A. 2013 May;161A(5):965-72. doi: 10.1002/ajmg.a.35749. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463464 Free PMC article.
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.
Suzuki S, Marazita ML, Cooper ME, Miwa N, Hing A, Jugessur A, Natsume N, Shimozato K, Ohbayashi N, Suzuki Y, Niimi T, Minami K, Yamamoto M, Altannamar TJ, Erkhembaatar T, Furukawa H, Daack-Hirsch S, L'heureux J, Brandon CA, Weinberg SM, Neiswanger K, Deleyiannis FW, de Salamanca JE, Vieira AR, Lidral AC, Martin JF, Murray JC. Suzuki S, et al. Among authors: suzuki y. Am J Hum Genet. 2009 Mar;84(3):406-11. doi: 10.1016/j.ajhg.2009.02.002. Epub 2009 Feb 26. Am J Hum Genet. 2009. PMID: 19249007 Free PMC article.
Granulocyte and Monocyte Adsorption Therapy in Patients With Sepsis: A Feasibility Study.
Nishida O, Nakamura T, Nakada T, Takahashi G, Masuda Y, Tsubouchi H, Kakihana Y, Sakamoto Y, Takasu O, Suzuki H, Nakazawa K, Kobayashi I, Doi K, Uchiyama S, Kitamura N, Kotani T, Kuriyama N, Hattori N, Suzuki Y, Tatsumi H, Moriyama K. Nishida O, et al. Among authors: suzuki y. Artif Organs. 2025 Jan 17. doi: 10.1111/aor.14943. Online ahead of print. Artif Organs. 2025. PMID: 39825588
Returning genetic risk information for hereditary cancers to participants in a population-based cohort study in Japan.
Ohneda K, Suzuki Y, Hamanaka Y, Tadaka S, Shimada M, Hasegawa-Minato J, Takahashi M, Fuse N, Nagami F, Kawame H, Kobayashi T, Yamaguchi-Kabata Y, Kinoshita K, Nakamura T, Ogishima S, Kumada K, Kudo H, Kuriyama SI, Izumi Y, Shimizu R, Tochigi M, Motonari T, Tokunaga H, Kikuchi A, Masamune A, Aoki Y, Ishioka C, Ishida T, Yamamoto M. Ohneda K, et al. Among authors: suzuki y. J Hum Genet. 2025 Jan 17. doi: 10.1038/s10038-024-01314-w. Online ahead of print. J Hum Genet. 2025. PMID: 39825003
Triple mosaic variants of PURA in a patient with multiple congenital anomalies.
Fujita A, Suenaga Y, Takeshita E, Takahashi Y, Suzuki Y, Ohori S, Tsuchida N, Uchiyama Y, Koshimizu E, Miyatake S, Mizuguchi T, Matsumoto N. Fujita A, et al. Among authors: suzuki y. J Hum Genet. 2025 Jan 14. doi: 10.1038/s10038-024-01315-9. Online ahead of print. J Hum Genet. 2025. PMID: 39809889
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