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

Aberrant One-Carbon Metabolism and Ancestral Genetics Underlie Edematous Severe Acute Malnutrition.

异常的一碳代谢和祖先遗传是水肿性严重急性营养不良的根本原因

Hanchard Neil, Lie Natasha, Han Yixing, Li Qing, Jajoo Aarti, Redmond Jared, Haldipur Aparna, Zewdu Solome, Banfield Emilyn, Swaminathan Shanker, Howell Sharon, Brown Orgen, Sadat Roa, Hall Nancy, Schulze Katharina, May Thaddaeus, Reid Marvin, Manary Mark, Trehan Indi, Mbiyavanga Mamana, Akurugu Wisdom, McKenzie Colin, Sengupta Dhriti, Atkinson Elizabeth, Choudhury Ananyo, Marshall Kwesi, Taylor-Bryan Carolyn

Edematous severe acute malnutrition is characterized by hypomethylation of DNA.

水肿性重度急性营养不良的特征是DNA低甲基化

Schulze Katharina V, Swaminathan Shanker, Howell Sharon, Jajoo Aarti, Lie Natasha C, Brown Orgen, Sadat Roa, Hall Nancy, Zhao Liang, Marshall Kwesi, May Thaddaeus, Reid Marvin E, Taylor-Bryan Carolyn, Wang Xueqing, Belmont John W, Guan Yongtao, Manary Mark J, Trehan Indi, McKenzie Colin A, Hanchard Neil A

Whole-Exome Sequencing Reveals Uncaptured Variation and Distinct Ancestry in the Southern African Population of Botswana

全外显子组测序揭示了博茨瓦纳南部非洲人群中未被发现的变异和独特的祖先构成

Retshabile, Gaone; Mlotshwa, Busisiwe C; Williams, Lesedi; Mwesigwa, Savannah; Mboowa, Gerald; Huang, Zhuoyi; Rustagi, Navin; Swaminathan, Shanker; Katagirya, Eric; Kyobe, Samuel; Wayengera, Misaki; Kisitu, Grace P; Kateete, David P; Wampande, Eddie M; Maplanka, Koketso; Kasvosve, Ishmael; Pettitt, Edward D; Matshaba, Mogomotsi; Nsangi, Betty; Marape, Marape; Tsimako-Johnstone, Masego; Brown, Chester W; Yu, Fuli; Kekitiinwa, Adeodata; Joloba, Moses; Mpoloka, Sununguko W; Mardon, Graeme; Anabwani, Gabriel; Hanchard, Neil A

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

一项针对先天性心血管左侧病变的全基因组关联研究显示,该病变与20号染色体上的一个基因位点相关。

Hanchard, Neil A; Swaminathan, Shanker; Bucasas, Kristine; Furthner, Dieter; Fernbach, Susan; Azamian, Mahshid S; Wang, Xueqing; Lewin, Mark; Towbin, Jeffrey A; D'Alessandro, Lisa C A; Morris, Shaine A; Dreyer, William; Denfield, Susan; Ayres, Nancy A; Franklin, Wayne J; Justino, Henri; Lantin-Hermoso, M Regina; Ocampo, Elena C; Santos, Alexia B; Parekh, Dhaval; Moodie, Douglas; Jeewa, Aamir; Lawrence, Emily; Allen, Hugh D; Penny, Daniel J; Fraser, Charles D; Lupski, James R; Popoola, Mojisola; Wadhwa, Lalita; Brook, J David; Bu'Lock, Frances A; Bhattacharya, Shoumo; Lalani, Seema R; Zender, Gloria A; Fitzgerald-Butt, Sara M; Bowman, Jessica; Corsmeier, Don; White, Peter; Lecerf, Kelsey; Zapata, Gladys; Hernandez, Patricia; Goodship, Judith A; Garg, Vidu; Keavney, Bernard D; Leal, Suzanne M; Cordell, Heather J; Belmont, John W; McBride, Kim L

Protective variant for hippocampal atrophy identified by whole exome sequencing

全外显子组测序鉴定出一种对海马萎缩具有保护作用的变异。

Nho, Kwangsik; Kim, Sungeun; Risacher, Shannon L; Shen, Li; Corneveaux, Jason J; Swaminathan, Shanker; Lin, Hai; Ramanan, Vijay K; Liu, Yunlong; Foroud, Tatiana M; Inlow, Mark H; Siniard, Ashley L; Reiman, Rebecca A; Aisen, Paul S; Petersen, Ronald C; Green, Robert C; Jack, Clifford R Jr; Weiner, Michael W; Baldwin, Clinton T; Lunetta, Kathryn L; Farrer, Lindsay A; Furney, Simon J; Lovestone, Simon; Simmons, Andrew; Mecocci, Patrizia; Vellas, Bruno; Tsolaki, Magda; Kloszewska, Iwona; Soininen, Hilkka; McDonald, Brenna C; Farlow, Martin R; Ghetti, Bernardino; Huentelman, Matthew J; Saykin, Andrew J

Characteristics of Bipolar I patients grouped by externalizing disorders

双相I型障碍患者外化障碍的特征

Swaminathan, Shanker; Koller, Daniel L; Foroud, Tatiana; Edenberg, Howard J; Xuei, Xiaoling; Niculescu, Alexander B 3rd; Nurnberger, John I Jr

Association of plasma and cortical amyloid beta is modulated by APOE ε4 status

血浆和皮质β淀粉样蛋白的结合受APOE ε4状态的调节

Swaminathan, Shanker; Risacher, Shannon L; Yoder, Karmen K; West, John D; Shen, Li; Kim, Sungeun; Inlow, Mark; Foroud, Tatiana; Jagust, William J; Koeppe, Robert A; Mathis, Chester A; Shaw, Leslie M; Trojanowski, John Q; Soares, Holly; Aisen, Paul S; Petersen, Ronald C; Weiner, Michael W; Saykin, Andrew J

Effect of complement CR1 on brain amyloid burden during aging and its modification by APOE genotype

补体CR1对衰老过程中脑淀粉样蛋白负荷的影响及其受APOE基因型调控

Thambisetty, Madhav; An, Yang; Nalls, Michael; Sojkova, Jitka; Swaminathan, Shanker; Zhou, Yun; Singleton, Andrew B; Wong, Dean F; Ferrucci, Luigi; Saykin, Andrew J; Resnick, Susan M

Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel.

利用多分析物检测方法研究遗传变异对老年人血浆蛋白水平的影响

Kim Sungeun, Swaminathan Shanker, Inlow Mark, Risacher Shannon L, Nho Kwangsik, Shen Li, Foroud Tatiana M, Petersen Ronald C, Aisen Paul S, Soares Holly, Toledo Jon B, Shaw Leslie M, Trojanowski John Q, Weiner Michael W, McDonald Brenna C, Farlow Martin R, Ghetti Bernardino, Saykin Andrew J

Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

阿尔茨海默病拷贝数变异分析:NIALOAD/NCRAD家族研究

Swaminathan, Shanker; Shen, Li; Kim, Sungeun; Inlow, Mark; West, John D; Faber, Kelley M; Foroud, Tatiana; Mayeux, Richard; Saykin, Andrew J