Functional Variants of the Lepr Gene in Patients With Hyperparathyroidism von Sue, G.R, Hoang, D, Li, A, Pizzoforato, N, Sosa, J.A, Roman, S.A, Dewan, A.T, Narayan, D

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A novel bioinformatics approach for identifying the genetic contributions to preeclampsia von Uzun, A, Dewan, A.T, Triche, E.W.T, Kurihara, S.I, Laliberte, A, Padbury, J.F

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472 Distribution of hidradenitis suppurativa monogenic etiologies in a racially diverse specialty clinic cohort von Colvin, A., Baugh, E., Babbush, K., Adriano, T., Benesh, G., Torpey, M.E., Nosrati, A., DeWan, A.T., Leal, S.M., Goldstein, D., Cohen, S., Petukhova, L.

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LB967 Monogenic mutations implicate STAT1 in hidradenitis suppurativa pathogenesis von Youssef, M., Baugh, E., Colvin, A., Babbush, K., Adriano, T., Benesh, G., Torpey, M.E., Nosrati, A., van Straalen, K.R., Tsoi, L.C., DeWan, A.T., Leal, S.M., Eisenberg, R., Gudjonsson, J.E., Milner, J., Cohen, S.R., Petukhova, L.

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Predictors of tanning dependence in white non‐Hispanic females and males von Cartmel, B., Bale, A.E., Mayne, S.T., Gelernter, J.E., DeWan, A.T., Spain, P., Leffell, D.J., Pagoto, S., Ferrucci, L.M.

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Mutations in the γ-Actin Gene ( ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) von Zhu, M., Yang, T., Wei, S., DeWan, A.T., Morell, R.J., Elfenbein, J.L., Fisher, R.A., Leal, S.M., Smith, R. J.H., Friderici, K.H.

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Supplementary Material for: Attempted Replication of 50 Reported Asthma Risk Genes Identifies a SNP in RAD50 as Associated with Childhood Atopic Asthma von Murk, W., Walsh, K., Hsu L.-I, Zhao, L., Bracken, M.B., DeWan, A.T.

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MSX measurements of BTH and ATH gravity waves and ATH polar mesospheric clouds von Stair, A.T., Humphrey, C.H., O'Neil, R., Picard, R.H., Dewan, E.M., Gardiner, H.A.B., Hegblom, E.R., Mill, J.

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