Introducing the Journal of the Medical Library Association's policy on the use of generative artificial intelligence in submissions

por Boruff, Jill T., Kraft, Michelle, Carroll, Alexander J.
Publicado 2023

Using information literacy to teach medical entrepreneurship and health care economics

por Carroll, Alexander J., Hallman, Shelby J., Umstead, Kelly A., McCall, James, DiMeo, Andrew J.
Publicado 2019

Building visualization skills through investigating the Journal of the Medical Library Association coauthorship network from 2006–2017

por Reznik-Zellen, Rebecca, Carroll, Alexander J., Harrington, Eileen G., Joubert, Douglas James, Nix, Tyler, Alpi, Kristine M.
Publicado 2020

Domains of professional practice: analysis of publications in the Journal of the Medical Library Association from 2010 to 2019

por Thompson, Holly J., Boruff, Jill T., Brown, Roy, Carroll, Alexander J., Cyrus, John W., Norton, Melanie J., Akers, Katherine G.
Publicado 2023

Rare coding variants in DNA damage repair genes associated with timing of natural menopause

por Ward, Lucas D., Parker, Margaret M., Deaton, Aimee M., Tu, Ho-Chou, Flynn-Carroll, Alexander O., Hinkle, Gregory, Nioi, Paul
Publicado 2021

Sphingosine kinase 2-deficiency mediated changes in spinal pain processing

por Canlas, Jastrow, Holt, Phillip, Carroll, Alexander, Rix, Shane, Ryan, Paul, Davies, Lorena, Matusica, Dusan, Pitson, Stuart M., Jessup, Claire F., Gibbins, Ian L., Haberberger, Rainer V.
Publicado 2015

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

por Deaton, Aimee M., Parker, Margaret M., Ward, Lucas D., Flynn-Carroll, Alexander O., BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A., Baras, Aris, Nioi, Paul
Publicado 2021

Striving for equity: An update from the Journal of the Medical Library Association

por Akers, Katherine G., Aaronson, Ellen M., Amos, Kathleen, Bartley, Kelsa, Carroll, Alexander J., Chambers, Thane, Cyrus, John W., Eldermire, Erin R. B., Linares, Brenda, Murphy, Beverly, Norton, Melanie J., Pionke, JJ, Reyes, Amy
Publicado 2021

GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

por Ward, Lucas D., Tu, Ho-Chou, Quenneville, Chelsea B., Tsour, Shira, Flynn-Carroll, Alexander O., Parker, Margaret M., Deaton, Aimee M., Haslett, Patrick A. J., Lotta, Luca A., Verweij, Niek, Ferreira, Manuel A. R., Baras, Aris, Hinkle, Gregory, Nioi, Paul
Publicado 2021

Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

por Parker, Margaret M., Damrauer, Scott M., Tcheandjieu, Catherine, Erbe, David, Aldinc, Emre, Hawkins, Philip N., Gillmore, Julian D., Hull, Leland E., Lynch, Julie A., Joseph, Jacob, Ticau, Simina, Flynn-Carroll, Alexander O., Deaton, Aimee M., Ward, Lucas D., Assimes, Themistocles L., Tsao, Philip S., Chang, Kyong-Mi, Rader, Daniel J., Fitzgerald, Kevin, Vaishnaw, Akshay K., Hinkle, Gregory, Nioi, Paul
Publicado 2021