SARS-CoV-2 receptor networks in diabetic and COVID-19–associated kidney disease von Menon, Rajasree, Otto, Edgar A., Sealfon, Rachel, Nair, Viji, Wong, Aaron K., Theesfeld, Chandra L., Chen, Xi, Wang, Yuan, Boppana, Avinash S., Luo, Jinghui, Yang, Yingbao, Kasson, Peter M., Schaub, Jennifer A., Berthier, Celine C., Eddy, Sean, Lienczewski, Chrysta C., Godfrey, Bradley, Dagenais, Susan L., Sohaney, Ryann, Hartman, John, Fermin, Damian, Subramanian, Lalita, Looker, Helen C., Harder, Jennifer L., Mariani, Laura H., Hodgin, Jeffrey B., Sexton, Jonathan Z., Wobus, Christiane E., Naik, Abhijit S., Nelson, Robert G., Troyanskaya, Olga G., Kretzler, Matthias

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Mutations in FOXC2 ( MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome von Fang, Jianming, Dagenais, Susan L., Erickson, Robert P., Arlt, Martin F., Glynn, Michael W., Gorski, Jerome L., Seaver, Laurie H., Glover, Thomas W.

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Estimation of DNA contamination and its sources in genotyped samples von Zajac, Gregory J. M., Fritsche, Lars G., Weinstock, Joshua S., Dagenais, Susan L., Lyons, Robert H., Brummett, Chad M., Abecasis, Gonçalo R.

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A Gata2 intronic enhancer confers its pan-endothelia-specific regulation von Khandekar, Melin, Brandt, William, Zhou, Yinghui, Dagenais, Susan, Glover, Thomas W, Suzuki, Norio, Shimizu, Ritsuko, Yamamoto, Masayuki, Lim, Kim-Chew, Engel, James Douglas

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Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2–q34.3 von Xu, Wenbo, Ahmad, Ayesha, Dagenais, Susan, Iyer, Ramaswamy K., Innis, Jeffrey W.

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FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome von Kriederman, Benjamin M., Myloyde, Teressa L., Witte, Marlys H., Dagenais, Susan L., Witte, Charles L., Rennels, Margaret, Bernas, Michael J., Lynch, Michelle T., Erickson, Robert P., Caulder, Mark S., Miura, Naoyuki, Jackson, David, Brooks, Brian P., Glover, Thomas W.

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A novel VEGFR3 mutation causes Milroy disease von Butler, Matthew G., Dagenais, Susan L., Rockson, Stanley G., Glover, Thomas W.

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The hepatocyte nuclear factor 3 α gene, HNF3α (FOXA1), on chromosome band 14q13 is amplified and overexpressed in esophageal and lung adenocarcinomas von LIN LIN, MILLER, Charles T, GLOVER, Thomas W, BEER, David G, CONTRERAS, Jorge I, PRESCOTT, Michael S, DAGENAIS, Susan L, RONG WU, YEE, John, ORRINGER, Mark B, MISEK, David E, HANASH, Samir M

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Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomuli... von Butler, Matthew G., Dagenais, Susan L., Garcia‐Perez, José L., Brouillard, Pascal, Vikkula, Miikka, Strouse, Peter, Innis, Jeffrey W., Glover, Thomas W.

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Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema–distichiasis syndrome von Dagenais, Susan L., Hartsough, Rebecca L., Erickson, Robert P., Witte, Marlys H., Butler, Matthew G., Glover, Thomas W.

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Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant von Lee, Jaekwon, Prohaska, Joseph R., Dagenais, Susan L., Glover, Thomas W., Thiele, Dennis J.

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Amplification and overexpression of the dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 (DYRK2) gene in esophageal and lung adenocarcinomas von MILLER, Charles T, AGGARWAL, Sanjeev, LIN, Theodore K, DAGENAIS, Susan L, CONTRERAS, Jorge I, ORRINGER, Mark B, GLOVER, Thomas W, BEER, David G, LIN LIN

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A Novel Frameshift Mutation in Exon 23 of ATP7A ( MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease von Dagenais, Susan L., Adam, Ayla N., Innis, Jeffrey W., Glover, Thomas W.

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Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice von Garnai, Sarah J, Brinkmeier, Michelle L, Emery, Ben, Aleman, Tomas S, Pyle, Louise C, Veleva-Rotse, Biliana, Sisk, Robert A, Rozsa, Frank W, Ozel, Ayse Bilge, Li, Jun Z, Moroi, Sayoko E, Archer, Steven M, Lin, Cheng-Mao, Sheskey, Sarah, Wiinikka-Buesser, Laurel, Eadie, James, Urquhart, Jill E, Black, Graeme C M, Othman, Mohammad I, Boehnke, Michael, Sullivan, Scot A, Skuta, Gregory L, Pawar, Hemant S, Katz, Alexander E, Huryn, Laryssa A, Hufnagel, Robert B, Camper, Sally A, Richards, Julia E, Prasov, Lev

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The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region von GLOVER, T. W, HOGE, A. W, MILLER, D. E, ASCARA-WILKE, J. E, ADAM, A. N, DAGENAIS, S. L, WILKE, C. M, DIERICK, H. A, BEER, D. G

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Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development von Brown, Nadean L, Dagenais, Susan L, Chen, Chuan-Min, Glaser, Tom

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Mutation of the FOXC2 gene in familial distichiasis von Brooks, Brian P, Dagenais, Susan L, Nelson, Christine C, Glynn, Michael W, Caulder, Mark S, Downs, Catherine A, Glover, Thomas W

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Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations von ERICKSON, Robert P, DAGENAIS, Susan L, WITTE, Marlys, GLOVER, Thomas W, CAULDER, Mark S, DOWNS, Catherine A, HERMAN, Gail, JONES, Marilyn C, KERSTJENS-FREDERIKSE, Wilhelmina S, LIDRAL, Andrew C, MCDONALD, Marie, NELSON, Christine C

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The canine copper toxicosis locus is not syntenic with ATP7B or ATX1 and maps to a region showing homology to human 2p21 von Dagenais, S L, Guevara-Fujita, M, Loechel, R, Burgess, A C, Miller, D E, Yuzbasiyan-Gurkan, V, Brewer, G J, Glover, T W

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Translocation breakpoints inFHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma von Fang, Jianming M., Arlt, Martin F., Burgess, Ann C., Dagenais, Susan L., Beer, David G., Glover, Thomas W.

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