Automated syndrome diagnosis by three-dimensional facial imaging

Authors: Hallgrímsson, Benedikt, Aponte, J. David, Katz, David C., Bannister, Jordan J., Riccardi, Sheri L., Mahasuwan, Nick, McInnes, Brenda L., Ferrara, Tracey M., Lipman, Danika M., Neves, Amanda B., Spitzmacher, Jared A.J., Larson, Jacinda R., Bellus, Gary A., Pham, Anh M., Aboujaoude, Elias, Benke, Timothy A., Chatfield, Kathryn C., Davis, Shanlee M., Elias, Ellen R., Enzenauer, Robert W., French, Brooke M., Pickler, Laura L., Shieh, Joseph T.C., Slavotinek, Anne, Harrop, A. Robertson, Innes, A. Micheil, McCandless, Shawn E., McCourt, Emily A., Meeks, Naomi J.L., Tartaglia, Nicole R., Tsai, Anne C.-H., Wyse, J. Patrick H., Bernstein, Jonathan A., Sanchez-Lara, Pedro A., Forkert, Nils D., Bernier, Francois P., Spritz, Richard A., Klein, Ophir D.

Source: In Genetics in Medicine October 2020 22(10):1682-1693

Integration and the Developmental Genetics of Allometry

Authors: Hallgrímsson, Benedikt, Katz, David C., Aponte, Jose D., Larson, Jacinda R., Devine, Jay, Gonzalez, Paula N., Young, Nathan M., Roseman, Charles C., Marcucio, Ralph S.

Source: Integrative and Comparative Biology, 2019 Nov 01. 59(5), 1369-1381.

Access URL: https://www.jstor.org/stable/26857002

Human Facial Shape and Size Heritability and Genetic Correlations.

Authors: Cole, Joanne B.¹, Manyama, Mange², Larson, Jacinda R.^3,4, Liberton, Denise K.^3,4, Ferrara, Tracey M.¹, Riccardi, Sheri L.¹, Mao Li⁵, Washington Mio⁵, Klein, Ophir D.^6,7,8, Santorico, Stephanie A.^1,9, Hallgrímsson, Benedikt^3,4, Spritz, Richard A.^1,10, richard.spritz@ucdenver.edu

Source: Genetics; Feb2017, Vol. 205 Issue 2, p967-978, 12p

Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape.

Authors: Cole, Joanne B.¹, Manyama, Mange², Kimwaga, Emmanuel², Mathayo, Joshua², Larson, Jacinda R.³, Liberton, Denise K.³, Lukowiak, Ken⁴, Ferrara, Tracey M.¹, Riccardi, Sheri L.¹, Li, Mao⁵, Mio, Washington⁵, Prochazkova, Michaela^6,7, Williams, Trevor⁸, Li, Hong⁸, Jones, Kenneth L.⁹, Klein, Ophir D.⁷, Santorico, Stephanie A.^1,10,11, Hallgrimsson, Benedikt³, Spritz, Richard A.^1,12, richard.spritz@ucdenver.edu

Source: PLoS Genetics; 8/25/2016, Vol. 12 Issue 8, p1-19, 19p

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Craniofacial morphometric analysis of individuals with X-linked hypohidrotic ectodermal dysplasia.

Authors: Goodwin, Alice F.¹, Larson, Jacinda R.^2,3, Jones, Kyle B.¹, Liberton, Denise K.², Landan, Maya¹, Wang, Zhifeng¹, Boekelheide, Anne⁴, Langham, Margaret⁴, Mushegyan, Vagan¹, Oberoi, Snehlata^1,4, Brao, Rosalie¹, Wen, Timothy¹, Johnson, Ramsey⁵, Huttner, Kenneth⁵, Grange, Dorothy K.⁶, Spritz, Richard A.⁷, Hallgrímsson, Benedikt^2,8, Jheon, Andrew H.^1,4, Klein, Ophir D.^1,4,9

Source: Molecular Genetics & Genomic Medicine. Sep2014, Vol. 2 Issue 5, p422-429. 8p.

Subject Terms: *DYSPLASIA, *CELLULAR pathology, *SEX chromosome abnormalities, *ECTODERMAL dysplasia, *HUMAN abnormalities

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