日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Recognition of a Critical Functional Domain and Improved PHOX2B Missense Variant Interpretation by Utilization of In Silico Prediction Tools

利用计算机预测工具识别关键功能域并改进PHOX2B错义变异的解读

Drackley, Andy; Skol, Andrew D; Rand, Casey M; Weese-Mayer, Debra E; Yap, Kai Lee

Development of an Atlas for US Pediatric Acute Care

美国儿科急症护理图谱的开发

Michelson, Kenneth A; Skol, Andrew D; Graves, John A; Remick, Katherine E; McMullen, Patrick D; Singamsetty, Naveen; Cory, Danielle K; Bucholz, Emily M

Network Analysis to Define Pediatric Acute Care Regions in Wisconsin

利用网络分析划分威斯康星州儿科急症护理区域

Michelson, Kenneth A; Remick, Katherine E; Bucholz, Emily M; McMullen, Patrick D; Singamsetty, Naveen; Skol, Andrew D; Cory, Danielle K; Graves, John A

GPR143-Associated Ocular Albinism in a Hispanic Family and Review of the Literature

西班牙裔家族中与 GPR143 相关的眼白化病及文献综述

Aneja, Anushree; Bohnsack, Brenda L; Allegretti, Valerie; Goetsch Weisman, Allison; Drackley, Andy; Ing, Alexander; McMullen, Patrick; Skol, Andrew; Ralay Ranaivo, Hantamalala; Yap, Kai Lee; Rathbun, Pamela; Gordon, Adam; Rossen, Jennifer L

Out-of-State Acute Care Use Among Pediatric Medicaid Enrollees

儿童医疗补助计划参保人员在州外接受急性护理的情况

Michelson, Kenneth A; Singamsetty, Naveen; Skol, Andrew D; Remick, Katherine E; Bucholz, Emily M; Graves, John A; Cory, Danielle K; McMullen, Patrick D

A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature Review

一例由C端DNA结合域新型MAF变异引起的非综合征型先天性白内障病例报告及文献综述

Zhao, Sharon H; Yap, Kai Lee; Allegretti, Valerie; Drackley, Andy; Ing, Alexander; Gordon, Adam; Skol, Andrew; McMullen, Patrick; Bohnsack, Brenda L; Kurup, Sudhi P; Ralay Ranaivo, Hantamalala; Rossen, Jennifer L

Inherited cancer predisposing mutations in patients with therapy-related myeloid neoplasms

治疗相关性髓系肿瘤患者的遗传性癌症易感突变

Shih, Andrew J; Jun, Tomi; Skol, Andrew D; Bao, Riyue; Huang, Lei; Vora, Sapana; McNerney, Megan E; Hungate, Eric A; Le Beau, Michelle M; Larson, Richard A; Elliott, Aaron; Lu, Hsiao-Mei; Huether, Robert; Hernandez, Felicia; Stölzel, Friedrich; Allan, James M; Onel, Kenan

Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

作者更正:全基因组关联研究鉴定出急性髓系白血病的易感基因位点

Lin, Wei-Yu; Fordham, Sarah E; Hungate, Eric; Sunter, Nicola J; Elstob, Claire; Xu, Yaobo; Park, Catherine; Quante, Anne; Strauch, Konstantin; Gieger, Christian; Skol, Andrew; Rahman, Thahira; Sucheston-Campbell, Lara; Wang, Junke; Hahn, Theresa; Clay-Gilmour, Alyssa I; Jones, Gail L; Marr, Helen J; Jackson, Graham H; Menne, Tobias; Collin, Mathew; Ivey, Adam; Hills, Robert K; Burnett, Alan K; Russell, Nigel H; Fitzgibbon, Jude; Larson, Richard A; Le Beau, Michelle M; Stock, Wendy; Heidenreich, Olaf; Alharbi, Abrar; Allsup, David J; Houlston, Richard S; Norden, Jean; Dickinson, Anne M; Douglas, Elisabeth; Lendrem, Clare; Daly, Ann K; Palm, Louise; Piechocki, Kim; Jeffries, Sally; Bornhäuser, Martin; Röllig, Christoph; Altmann, Heidi; Ruhnke, Leo; Kunadt, Desiree; Wagenführ, Lisa; Cordell, Heather J; Darlay, Rebecca; Andersen, Mette K; Fontana, Maria C; Martinelli, Giovanni; Marconi, Giovanni; Sanz, Miguel A; Cervera, José; Gómez-Seguí, Inés; Cluzeau, Thomas; Moreilhon, Chimène; Raynaud, Sophie; Sill, Heinz; Voso, Maria Teresa; Lo-Coco, Francesco; Dombret, Hervé; Cheok, Meyling; Preudhomme, Claude; Gale, Rosemary E; Linch, David; Gaal-Wesinger, Julia; Masszi, Andras; Nowak, Daniel; Hofmann, Wolf-Karsten; Gilkes, Amanda; Porkka, Kimmo; Milosevic Feenstra, Jelena D; Kralovics, Robert; Grimwade, David; Meggendorfer, Manja; Haferlach, Torsten; Krizsán, Szilvia; Bödör, Csaba; Stölzel, Friedrich; Onel, Kenan; Allan, James M

PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors

PIK3R5基因预测VEGF通路抑制剂诱发的高血压

Quintanilha, Julia C F; Racioppi, Alessandro; Wang, Jin; Etheridge, Amy S; Denning, Stefanie; Peña, Carol E; Skol, Andrew D; Crona, Daniel J; Lin, Danyu; Innocenti, Federico

Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

全基因组关联研究鉴定出急性髓系白血病的易感基因位点

Lin, Wei-Yu; Fordham, Sarah E; Hungate, Eric; Sunter, Nicola J; Elstob, Claire; Xu, Yaobo; Park, Catherine; Quante, Anne; Strauch, Konstantin; Gieger, Christian; Skol, Andrew; Rahman, Thahira; Sucheston-Campbell, Lara; Wang, Junke; Hahn, Theresa; Clay-Gilmour, Alyssa I; Jones, Gail L; Marr, Helen J; Jackson, Graham H; Menne, Tobias; Collin, Mathew; Ivey, Adam; Hills, Robert K; Burnett, Alan K; Russell, Nigel H; Fitzgibbon, Jude; Larson, Richard A; Le Beau, Michelle M; Stock, Wendy; Heidenreich, Olaf; Alharbi, Abrar; Allsup, David J; Houlston, Richard S; Norden, Jean; Dickinson, Anne M; Douglas, Elisabeth; Lendrem, Clare; Daly, Ann K; Palm, Louise; Piechocki, Kim; Jeffries, Sally; Bornhäuser, Martin; Röllig, Christoph; Altmann, Heidi; Ruhnke, Leo; Kunadt, Desiree; Wagenführ, Lisa; Cordell, Heather J; Darlay, Rebecca; Andersen, Mette K; Fontana, Maria C; Martinelli, Giovanni; Marconi, Giovanni; Sanz, Miguel A; Cervera, José; Gómez-Seguí, Inés; Cluzeau, Thomas; Moreilhon, Chimène; Raynaud, Sophie; Sill, Heinz; Voso, Maria Teresa; Lo-Coco, Francesco; Dombret, Hervé; Cheok, Meyling; Preudhomme, Claude; Gale, Rosemary E; Linch, David; Gaal-Wesinger, Julia; Masszi, Andras; Nowak, Daniel; Hofmann, Wolf-Karsten; Gilkes, Amanda; Porkka, Kimmo; Milosevic Feenstra, Jelena D; Kralovics, Robert; Grimwade, David; Meggendorfer, Manja; Haferlach, Torsten; Krizsán, Szilvia; Bödör, Csaba; Stölzel, Friedrich; Onel, Kenan; Allan, James M