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Preventing Chronic Disease|May 13, 2022
Development of a Field Guide for Assessing Readiness to Implement Evidence-Based Cancer Screening Interventions in Primary Care ClinicsSarah D Hohl, Stephanie Melillo, Thuy T Vu, et al.
The Journal of Investigative Dermatology|March 12, 2002
Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenitaA Terrinoni, F J Smith, B Didona, et al.
Psychiatric Services (Washington, D.C.)|May 4, 2021
"What Will Happen If I Say Yes?" Perspectives on a Standardized Firearm Access Question Among Adults With Depressive SymptomsJulie E Richards, Sarah D Hohl, Courtney D Segal, et al.
American Journal of Public Health|January 23, 2016
Characterizing Community Health Workers on Research Teams: Results From the Centers for Population Health and Health DisparitiesSarah D Hohl, Beti Thompson, Jessica L Krok-Schoen, et al.
The British Journal of Dermatology|May 15, 2009
Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogsK M Credille, J S Minor, K F Barnhart, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticumL Cai, A Lumsden, U P Guenther, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Cancer Causes & Control : CCC|January 17, 2026
Perspectives on GUIDE (Guiding participation toward understanding, inclusion, diversity, and equity for cancer trials): a clinical trial access interventionKristine A Karvonen, Jean A McDougall, Sarah D Hohl, et al.
Journal of General Internal Medicine|July 27, 2019
If You Listen, I Will Talk: the Experience of Being Asked About Suicidality During Routine Primary CareJulie E Richards, Sarah D Hohl, Ursula Whiteside, et al.
The Journal of Cell Biology|October 19, 2000
Lessons from loricrin-deficient mice: compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope proteinP J Koch, P A de Viragh, E Scharer, et al.
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