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

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

对先前已知的与慢性抽动症相关的遗传变异进行研究:一种传递不平衡检验方法

Abdulkadir, Mohamed; Londono, Douglas; Gordon, Derek; Fernandez, Thomas V; Brown, Lawrence W; Cheon, Keun-Ah; Coffey, Barbara J; Elzerman, Lonneke; Fremer, Carolin; Fründt, Odette; Garcia-Delgar, Blanca; Gilbert, Donald L; Grice, Dorothy E; Hedderly, Tammy; Heyman, Isobel; Hong, Hyun Ju; Huyser, Chaim; Ibanez-Gomez, Laura; Jakubovski, Ewgeni; Kim, Young Key; Kim, Young Shin; Koh, Yun-Joo; Kook, Sodahm; Kuperman, Samuel; Leventhal, Bennett; Ludolph, Andrea G; Madruga-Garrido, Marcos; Maras, Athanasios; Mir, Pablo; Morer, Astrid; Müller-Vahl, Kirsten; Münchau, Alexander; Murphy, Tara L; Plessen, Kerstin J; Roessner, Veit; Shin, Eun-Young; Song, Dong-Ho; Song, Jungeun; Tübing, Jennifer; van den Ban, Els; Visscher, Frank; Wanderer, Sina; Woods, Martin; Zinner, Samuel H; King, Robert A; Tischfield, Jay A; Heiman, Gary A; Hoekstra, Pieter J; Dietrich, Andrea

An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance.

在多效性遗传模式下,遗传关联研究的功效和样本量计算的解析解

Gordon Derek, Londono Douglas, Patel Payal, Kim Wonkuk, Finch Stephen J, Heiman Gary A

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

利用贝叶斯后验概率将基因与纵向表型联系起来

Musolf, Anthony; Nato, Alejandro Q Jr; Londono, Douglas; Zhou, Lisheng; Matise, Tara C; Gordon, Derek

TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

TDT-HET:一种新的传递不平衡检验,它将基因座异质性纳入基于家庭的关联数据分析中。

Londono, Douglas; Buyske, Steven; Finch, Stephen J; Sharma, Swarkar; Wise, Carol A; Gordon, Derek

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

IL-18R1 和 IL-18RAP 的 SNP 可能与非裔美国婴儿的支气管肺发育不良有关。

Floros, Joanna; Londono, Douglas; Gordon, Derek; Silveyra, Patricia; Diangelo, Susan L; Viscardi, Rose M; Worthen, George S; Shenberger, Jeffrey; Wang, Guirong; Lin, Zhenwu; Thomas, Neal J

Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error

用于检测遗传关联的单变量和多变量趋势检验,结合新一代测序技术,对测序误差具有鲁棒性。

Kim, Wonkuk; Londono, Douglas; Zhou, Lisheng; Xing, Jinchuan; Nato, Alejandro Q; Musolf, Anthony; Matise, Tara C; Finch, Stephen J; Gordon, Derek

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes

全基因组关联研究提示青少年特发性脊柱侧弯的候选易感基因

Sharma, Swarkar; Gao, Xiaochong; Londono, Douglas; Devroy, Shonn E; Mauldin, Kristen N; Frankel, Jessica T; Brandon, January M; Zhang, Dongping; Li, Quan-Zhen; Dobbs, Matthew B; Gurnett, Christina A; Grant, Struan F A; Hakonarson, Hakon; Dormans, John P; Herring, John A; Gordon, Derek; Wise, Carol A

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

EDNRA 变异与平滑肌 mRNA 水平、细胞增殖率和囊性纤维化肺病严重程度相关。

Darrah, Rebecca; McKone, Edward; O'Connor, Clare; Rodgers, Christine; Genatossio, Alan; McNamara, Sharon; Gibson, Ronald; Stuart Elborn, J; Ennis, Madeleine; Gallagher, Charles G; Kalsheker, Noor; Aitken, Moira; Wiese, Dawn; Dunn, John; Smith, Paul; Pace, Rhonda; Londono, Douglas; Goddard, Katrina A B; Knowles, Michael R; Drumm, Mitchell L

Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians

证据表明,伤害感受素/孤啡肽FQ受体基因OPRL1的两种变体与白种人阿片类药物成瘾的易感性相关

Briant, Judith A; Nielsen, David A; Proudnikov, Dmitri; Londono, Douglas; Ho, Ann; Ott, Jurg; Kreek, Mary Jeanne

Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata

全基因组连锁分析揭示了斑秃的多个易感基因位点

Martinez-Mir, Amalia; Zlotogorski, Abraham; Gordon, Derek; Petukhova, Lynn; Mo, Jianhong; Gilliam, T Conrad; Londono, Douglas; Haynes, Chad; Ott, Jurg; Hordinsky, Maria; Nanova, Krassimira; Norris, David; Price, Vera; Duvic, Madeleine; Christiano, Angela M