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

Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多族裔全基因组分析鉴定出与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Arehart, Christopher H; Evans, Luke M; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; Edris, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta R; Brumpton, Ben M; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan A; Sanders, Alan R; Whiteman, David C; MacGregor, Stuart; Medland, Sarah E; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlinger, Gregory; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle L; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin G; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zöllner, Sebastian; Verma, Anurag; Preuss, Michael H; Kenny, Eimear; Hendricks, Audrey E; Fishbein, Lauren; Kraft, Peter; Daly, Mark J; Neale, Benjamin M; Martin, Alicia R; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Long-Term Outcomes of Patients Diagnosed With Differentiated Thyroid Cancer in Childhood and Young Adulthood

儿童期和青年期诊断为分化型甲状腺癌患者的长期预后

Valenciaga, Anisley; Liyanarachchi, Sandya; Brock, Pamela L; Ringel, Matthew D

2025 American Thyroid Association Management Guidelines for Adult Patients with Differentiated Thyroid Cancer

2025年美国甲状腺协会成人分化型甲状腺癌管理指南

Ringel, Matthew D; Sosa, Julie Ann; Baloch, Zubair; Bischoff, Lindsay; Bloom, Gary; Brent, Gregory A; Brock, Pamela L; Chou, Roger; Flavell, Robert R; Goldner, Whitney; Grubbs, Elizabeth G; Haymart, Megan; Larson, Steven M; Leung, Angela M; Osborne, Joseph R; Ridge, John A; Robinson, Bruce; Steward, David L; Tufano, Ralph P; Wirth, Lori J

Predicting heart failure in phospholamban p.(Arg14del)-positive individuals using vectorcardiographic information

利用向量心电图信息预测磷蛋白p.(Arg14del)阳性个体的心力衰竭

Brock, Pamela; Sevigny, Myriam; Liyanarachchi, Sandya; Comiskey, Daniel F Jr; Li, Wei; Saarinen, Saila; Yilmaz, Ayse Selen; Nieminen, Anni I; Ringel, Matthew D; Peltomäki, Päivi; Ollila, Saara; Nieminen, Taina T; Van Der Heide, M Y C; Verstraelen, T E; De Brouwer, R; Van Drie, E; Houweling, A C; Dickhoff, C; Germans, T; Meems, L M G; Te Riele, A S J M; Van Spaendonck-Zwarts, K Y; Cox, M G P J; Van Tintelen, J P; Kors, J A; Postema, P G; Wilde, A A M

Germline POT1 Variants in a Pan-Cancer Cohort

泛癌队列中的种系 POT1 变异

Brock, Pamela L; Webster, Morgan; Liyanarachchi, Sandya; Byrne, Lindsey; Hedges, Dale J; Gulhati, Pat; Hicks, J Kevin; Chan, Carlos H F; Onel, Kenan; Stout, Leigh Anne; Maxwell, Whitney; Pickarski, Justine Cooper; Estrada-Veras, Juvianee; Salhia, Bodour; Axell, Lisen; Holman, Laura L; Abdel-Rahman, Mohamed H; Ringel, Matthew D

Call to action for genetic counseling research in hereditary cancer: Considerations from the evidence-based guidelines development process

呼吁开展遗传性癌症的遗传咨询研究:循证指南制定过程的考量

Levin, Brooke; Salo-Mullen, Erin; Culver, Julie O; Kurz, Raluca N; Brock, Pamela; Demsky, Rochelle; Lloyd, Stacy; Lopez, Ghecemy; Mai, Phuong L; Wolfe Schneider, Kami

Diagnosing Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome and a Novel GATA3 Variant

诊断甲状旁腺功能减退症、感觉神经性耳聋、肾发育不良综合征和一种新的GATA3变异

Valenciaga, Anisley; Brock, Pamela; O'Donnell, Benjamin; Ing, Steven W

Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多民族遗传学研究阐明了与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; EdrisMohammed, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta Riise; Brumpton, Ben; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan; Sanders, Alan R; Whiteman, David; MacGregor, Stuart; Medland, Sarah; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlingeer, Greg; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zoellner, Sebastian; Verma, Anurag; Preuss, Michael; Kenny, Eimear; Hendricks, Audrey; Fishbein, Lauren; Kraft, Peter; Daly, Mark; Neale, Benjamin; Martin, Alicia; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Early-Onset Sarcoma With Germline MAX Variant: Expanding the Spectrum in Hereditary Pheochromocytoma and Paraganglioma

携带种系MAX变异的早发性肉瘤:扩展遗传性嗜铬细胞瘤和副神经节瘤的谱系

Eren, Aysegul; Brock, Pamela L; Dedhia, Priya H

Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype

端粒延长基因的种系变异易导致一种综合征型乳头状甲状腺癌。

DeBoy, Emily A; Nicosia, Anna M; Liyanarachchi, Sandya; Iyer, Sheila S; Shah, Manisha H; Ringel, Matthew D; Brock, Pamela; Armanios, Mary