Haplotype inference in general pedigrees with two sites

por Doan, Duong D, Evans, Patricia A
Publicado 2011

An FPT haplotyping algorithm on pedigrees with a small number of sites

por Doan, Duong D, Evans, Patricia A
Publicado 2011

Regulatory link mapping between organisms

por Sharma, Rachita, Evans, Patricia A, Bhavsar, Virendrakumar C
Publicado 2011

A Free Parking Trial to Increase Visitation and Improve Extremely Low Birth Weight Infant Outcomes

por Northrup, Thomas F., Evans, Patricia W., Lillie, Margaret L., Tyson, Jon E.
Publicado 2016

Residual erythropoiesis protects against myocardial hemosiderosis in transfusion-dependent thalassemia by lowering labile plasma iron via transient generation of apotransferrin

por Garbowski, Maciej W., Evans, Patricia, Vlachodimitropoulou, Evangelia, Hider, Robert, Porter, John B.
Publicado 2017

Electroencephalographic (EEG) Biomarkers in Genetic Neurodevelopmental Disorders

por Goodspeed, Kimberly, Armstrong, Dallas, Dolce, Alison, Evans, Patricia, Said, Rana, Tsai, Peter, Sirsi, Deepa
Publicado 2023

Hepcidin and iron species distribution inside the first-trimester human gestational sac

por Evans, Patricia, Cindrova-Davies, Tereza, Muttukrishna, Shanthi, Burton, Graham J., Porter, John, Jauniaux, Eric
Publicado 2011

Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability

por Grau, Christina, Starkovich, Molly, Azamian, Mahshid S., Xia, Fan, Cheung, Sau Wai, Evans, Patricia, Henderson, Alex, Lalani, Seema R., Scott, Daryl A.
Publicado 2017

Treatment of heart failure in adults with thalassemia major: response in patients randomised to deferoxamine with or without deferiprone

por Porter, John B, Wood, John, Olivieri, Nancy, Vichinsky, Elliott P, Taher, Ali, Neufeld, Ellis, Giardina, Patricia, Thompson, Alexis, Moore, Blaine, Evans, Patricia, Kim, Hae-Young, Macklin, Eric A, Trachtenberg, Felicia
Publicado 2013

Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants

por Tuncay, Islam Oguz, Parmalee, Nancy L., Khalil, Raida, Kaur, Kiran, Kumar, Ashwani, Jimale, Mohamed, Howe, Jennifer L., Goodspeed, Kimberly, Evans, Patricia, Alzghoul, Loai, Xing, Chao, Scherer, Stephen W., Chahrour, Maria H.
Publicado 2022

A Patient-Centered Environmental Scan of Inpatient Visitor Policies During the COVID-19 Pandemic

por Harrison, James D, Weiss, Rachel, Radhakrishnan, Nila S, Hanson, Catherine, Carnie, Martha B, Evans, Patricia, Banta, Jim, Symczak, Gina, Ziegler, Georgiann, Holmes, D’Anna, Michel-Leconte, Safia J, Rogers, Beverly, Wurst, Melissa, Alikhaani, Jacqueline, Davis, Clark, Lee, Tiffany, Schnipper, Jeffrey L, Auerbach, Andrew D, Romond, John
Publicado 2021

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype

por Adams, Paul, Altes, Albert, Brissot, Pierre, Butzeck, Barbara, Cabantchik, Ioav, Cançado, Rodolfo, Distante, Sonia, Evans, Patricia, Evans, Robert, Ganz, Tomas, Girelli, Domenico, Hultcrantz, Rolf, McLaren, Gordon, Marris, Ben, Milman, Nils, Nemeth, Elizabeta, Nielsen, Peter, Pineau, Brigitte, Piperno, Alberto, Porto, Graça, Prince, Dianne, Ryan, John, Sanchez, Mayka, Santos, Paulo, Swinkels, Dorine, Teixeira, Emerência, Toska, Ketil, Vanclooster, Annick, White, Desley
Publicado 2018