Michael Lyons to Pedigree
This is a "connection" page, showing publications Michael Lyons has written about Pedigree.
Connection Strength
0.749
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Larrew T, Eskandari R, Holden KR, Chen A, Spellicy CJ, Jones JR, Lee JA, Lyons MJ. Transgenerational Inheritance of Familial Lipomyelomeningocele. J Child Neurol. 2017 Dec; 32(14):1118-1122.
Score: 0.558
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Crider A, Kremen WS, Xian H, Jacobson KC, Waterman B, Eisen SA, Tsuang MT, Lyons MJ. Stability, consistency, and heritability of electrodermal response lability in middle-aged male twins. Psychophysiology. 2004 Jul; 41(4):501-9.
Score: 0.055
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Parenti I, Lehalle D, Nava C, Torti E, Leit?o E, Person R, Mizuguchi T, Matsumoto N, Kato M, Nakamura K, de Man SA, Cope H, Shashi V, Friedman J, Joset P, Steindl K, Rauch A, Muffels I, van Hasselt PM, Petit F, Smol T, Le Guyader G, Bilan F, Sorlin A, Vitobello A, Philippe C, van de Laar IMBH, van Slegtenhorst MA, Campeau PM, Au PYB, Nakashima M, Saitsu H, Yamamoto T, Nomura Y, Louie RJ, Lyons MJ, Dobson A, Plomp AS, Motazacker MM, Kaiser FJ, Timberlake AT, Fuchs SA, Depienne C, Mignot C. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy. Hum Genet. 2021 Jul; 140(7):1109-1120.
Score: 0.044
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Lee YR, Khan K, Armfield-Uhas K, Srikanth S, Thompson NA, Pardo M, Yu L, Norris JW, Peng Y, Gripp KW, Aleck KA, Li C, Spence E, Choi TI, Kwon SJ, Park HM, Yu D, Heo WD, Mooney MR, Baig SM, Wentzensen IM, Telegrafi A, McWalter K, Moreland T, Roadhouse C, Ramsey K, Lyons MJ, Skinner C, Alexov E, Katsanis N, Stevenson RE, Choudhary JS, Adams DJ, Kim CH, Davis EE, Schwartz CE. Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nat Commun. 2020 07 23; 11(1):3698.
Score: 0.042
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Docherty AR, Kremen WS, Panizzon MS, Prom-Wormley EC, Franz CE, Lyons MJ, Eaves LJ, Neale MC. Comparison of Twin and Extended Pedigree Designs for Obtaining Heritability Estimates. Behav Genet. 2015 Jul; 45(4):461-6.
Score: 0.029
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Clark RD, Graham JM, Friez MJ, Hoo JJ, Jones KL, McKeown C, Moeschler JB, Raymond FL, Rogers RC, Schwartz CE, Battaglia A, Lyons MJ, Stevenson RE. FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing. Genet Med. 2009 Nov; 11(11):769-75.
Score: 0.020