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

Generalisability of Maternal Genetic Risk Score for Birth Weight Across Racial Identity and Ancestry: A Secondary Analysis of a Prospective Cohort Study

母体遗传风险评分对出生体重的普遍适用性:一项前瞻性队列研究的二次分析

Tristani-Firouzi, Bita; Pappas, Lisa; Joseph, Merry; Zeinomar, Maryam; Debbink, Michelle P; Mims, Joseph; Guerrero, Rafael; Moore, Barry; Silver, Robert M; Workalemahu, Tsegaselassie; Haas, David; Steller, Jonathan G; Saade, George; Blue, Nathan R

Protection from Chronic Musculoskeletal Pain: A Scoping Review

预防慢性肌肉骨骼疼痛:范围综述

Moore, Barry E; Schleidgen, Leon; Hang, Chan P; Chelsea, Hung C Y; Rabey, Martin; Ng, Leo; Chai, Kevin E K; Melton, Phillip; Cowen, Gill; Beales, Darren; Moloney, Niamh

Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associations

利用SimPheny进行表型优先的患者匹配,可以识别出除已筛选基因关联之外的诊断候选基因。

Cooperstein, Isabelle B; Ward, Alistair; Kobren, Shilpa N; Lebleu, Emerson; Moore, Barry; Spillmann, Rebecca C; Shashi, Vandana; Marth, Gabor T

Breast Cancer Is Increased in Women With Primary Ovarian Insufficiency

原发性卵巢功能不全的女性患乳腺癌的风险增加

Allen-Brady, Kristina; Moore, Barry; Verrilli, Lauren E; Alvord, Margaret A; Kern, Marina; Camp, Nicola; Kelley, Kristen; Letourneau, Joseph; Cannon-Albright, Lisa; Yandell, Mark; Johnstone, Erica B; Welt, Corrine K

The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit

犹他州NeoSeq项目:一项旨在促进新生儿重症监护病房基因组诊断的多学科合作项目

Malone Jenkins, Sabrina; Palmquist, Rachel N; Moore, Barry; Boyden, Steven E; Nicholas, Thomas J; Bayrak-Toydemir, Pinar; Mao, Rong; Farrell, J Andrew R; Holt, Carson H; Rynearson, Shawn G; Solorzano, Chelsea M; Ward, Alistair; Best, D Hunter; Al-Sweel, Najla; Bentley, Dawn L; Brunelli, Luca; Chow, Clement Y; Close, Devin W; Cormier, Michael J; Deshotel, Malia J; Durtschi, Jacob; Eide, Erik J; Floyd, Luaiva; Fredrickson, Eric K; Fulmer, Makenzie L; Hernandez, Edgar J; Kapron, Ashley L; Karren, Mary Anne; Lewis, Robert G; Miller, Christine E; Murtaugh, L Charles; Nicholson, Kelsey E; Noble, Katherine; O'Fallon, Brendan D; O'Shea, John M; Pattison, David C; Pedersen, Brent S; Petersen, Brandy J; Peterson, Bennet D; Pizzo, Lucilla; Reynolds, Hayley M; Rindler, Paul; Torr, Carrie B; Wen, Ting; Yost, H Joseph; Zhao, Jian; Yandell, Mark; Marth, Gabor T; Quinlan, Aaron R; Carey, John C; Shayota, Brian J; Tristani-Firouzi, Martin; Bonkowsky, Joshua L

MPSE identifies newborns for whole genome sequencing within 48 h of NICU admission

MPSE可在新生儿重症监护室入院48小时内识别需要进行全基因组测序的新生儿。

Peterson, Bennet; Juarez, Edwin F; Moore, Barry; Hernandez, Edgar Javier; Frise, Erwin; Li, Jianrong; Lussier, Yves; Tristani-Firouzi, Martin; Reese, Martin G; Malone Jenkins, Sabrina; Kingsmore, Stephen F; Bainbridge, Matthew N; Yandell, Mark

Health care professionals' attitudes, behaviours and barriers toward exercise promotion among patients: A systematic review

医护人员对促进患者运动的态度、行为和障碍:一项系统性综述

Avsar, Pinar; Moore, Zena; Nasaif, Husain; Moore, Barry; Patton, Declan; O'Connor, Tom; Renjith, Vishnu

Use of a Maternal Genetic Risk Score to Derive and Test a Genetically Customized Fetal Growth Curve

利用母体遗传风险评分推导和检验基因定制的胎儿生长曲线

Joseph, Merry; Pappas, Lisa; Guerrero, Rafael; Zeinomar, Maryam; Mims, Joseph R Jr; Moore, Barry; Workalemahu, Tsegaselassie; Scifres, Christina; Steller, Jon G; Saade, George; Silver, Robert M; Blue, Nathan R

Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks

对婴儿猝死综合征进行基因组与环境交叉分析,揭示了病因的异质性以及大麻和遗传疾病的显著风险。

Kingsmore, Stephen F; Bandoli, Gretchen; Helbling, Daniel C; Baer, Rebecca; Blincow, Eric; Cao, Bryant; Frise, Erwin; Heinen, Alaina; Jelliffe-Pawlowski, Laura; Kobayashi, Erica Sanford; Kraan, Lucita Van Der; Kwon, Hugh; Lavy, Rishona; Moore, Barry; Oh, Danny; Oltman, Scott; Eric Ontiveros; Protopsaltis, Liana; Yandell, Mark; Chambers, Christina D

Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.

通过基于纯化超选择的联邦训练,对基于基因组的新生儿筛查进行严重儿童遗传疾病的预认证

Kingsmore Stephen F, Wright Meredith, Smith Laurie D, Liang Yupu, Mowrey William R, Protopsaltis Liana, Bainbridge Matthew, Baker Mei, Batalov Sergey, Blincow Eric, Cao Bryant, Caylor Sara, Chambers Christina, Ellsworth Katarzyna, Feigenbaum Annette, Frise Erwin, Guidugli Lucia, Hall Kevin P, Hansen Christian, Kiel Mark, Van Der Kraan Lucita, Krilow Chad, Kwon Hugh, Madhavrao Lakshminarasimha, Lefebvre Sebastien, Leipzig Jeremy, Mardach Rebecca, Moore Barry, Oh Danny, Olsen Lauren, Ontiveros Eric, Owen Mallory J, Reimers Rebecca, Scharer Gunter, Schleit Jennifer, Shelnutt Seth, Mehtalia Shyamal S, Oriol Albert, Sanford Erica, Schwartz Steve, Wigby Kristen, Willis Mary J, Yandell Mark, Kunard Chris M, Defay Thomas