1. A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program. Issue 10 (16th April 2021) Authors: Stilp, Adrienne M; Emery, Leslie S; Broome, Jai G; Buth, Erin J; Khan, Alyna T; Laurie, Cecelia A; Wang, Fei Fei; Wong, Quenna; Chen, Dongquan; D'Augustine, Catherine M; Heard-Costa, Nancy L; Hohensee, Chancellor R; Johnson, William Craig; Juarez, Lucia D; Liu, Jingmin; Mutalik, Karen M; Raffield... Journal: American journal of epidemiology Issue: Volume 190:Issue 10(2021) Page Start: 1977 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population. Issue 9 (9th March 2021) Authors: Sun, Pengfei; Zhou, Wei; Fu, Yi; Cheung, Chloe Y Y; Dong, Yujun; Yang, Min-Lee; Zhang, He; Jia, Jia; Huo, Yong; Willer, Cristen J; Chen, Y Eugene; Tang, Clara S; Tse, Hung-Fat; Lam, Karen S L; Gao, Wei; Xu, Ming; Yu, Haiyi; Sham, Pak Chung; Zhang, Yan; Ganesh, Santhi K Journal: Human molecular genetics Issue: Volume 30:Issue 9(2021) Page Start: 836 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Bilateral internal mammary artery fibromuscular dysplasia discovered upon evaluation for reconstructive breast surgery. (October 2015) Authors: Heidt, Steven T; Ganesh, Santhi K; Liu, Peter; Froehlich, James B; Kline-Rogers, Eva Journal: Vascular medicine Issue: Volume 20:Number 5(2015:Oct.) Page Start: 487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia. Issue 1 (19th March 2021) Authors: Persu, Alexandre; Dobrowolski, Piotr; Gornik, Heather L; Olin, Jeffrey W; Adlam, David; Azizi, Michel; Boutouyrie, Pierre; Bruno, Rosa Maria; Boulanger, Marion; Demoulin, Jean-Baptiste; Ganesh, Santhi K; J. Guzik, Tomasz; Januszewicz, Magdalena; Kovacic, Jason C; Kruk, Mariusz; de Leeuw, Peter; L... Journal: Cardiovascular research Issue: Volume 118:Issue 1(2022) Page Start: 65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. First International Consensus on the diagnosis and management of fibromuscular dysplasia. (April 2019) Authors: Gornik, Heather L; Persu, Alexandre; Adlam, David; Aparicio, Lucas S; Azizi, Michel; Boulanger, Marion; Bruno, Rosa Maria; de Leeuw, Peter; Fendrikova-Mahlay, Natalia; Froehlich, James; Ganesh, Santhi K; Gray, Bruce H; Jamison, Cathlin; Januszewicz, Andrzej; Jeunemaitre, Xavier; Kadian-Dodov, Dan... Journal: Vascular medicine Issue: Volume 24:Number 2(2019) Page Start: 164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study. Issue 20 (2nd March 2022) Authors: Portilla-Fernandez, Eliana; Klarin, Derek; Hwang, Shih-Jen; Biggs, Mary L; Bis, Joshua C; Weiss, Stefan; Rospleszcz, Susanne; Natarajan, Pradeep; Hoffmann, Udo; Rogers, Ian S; Truong, Quynh A; Völker, Uwe; Dörr, Marcus; Bülow, Robin; Criqui, Michael H; Allison, Matthew; Ganesh, Santhi K; Yao, Jie... Journal: Human molecular genetics Issue: Volume 31:Issue 20(2022) Page Start: 3566 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular genetic evaluation of pediatric renovascular hypertension due to renal artery stenosis and abdominal aortic coarctation in neurofibromatosis type 1. Issue 3 (2nd September 2021) Authors: Coleman, Dawn M; Wang, Yu; Yang, Min-Lee; Hunker, Kristina L; Birt, Isabelle; Bergin, Ingrid L; Li, Jun Z; Stanley, James C; Ganesh, Santhi K Journal: Human molecular genetics Issue: Volume 31:Issue 3(2022) Page Start: 334 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Issue 4 (12th June 2020) Authors: Georges, Adrien; Albuisson, Juliette; Berrandou, Takiy; Dupré, Délia; Lorthioir, Aurélien; D'Escamard, Valentina; Di Narzo, Antonio F; Kadian-Dodov, Daniella; Olin, Jeffrey W; Warchol-Celinska, Ewa; Prejbisz, Aleksander; Januszewicz, Andrzej; Bruneval, Patrick; Baranowska, Anna A; Webb, Tom R; Ha... Journal: Cardiovascular research Issue: Volume 117:Issue 4(2021) Page Start: 1154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. S-22-4: GENOME WIDE ASSOCIATION STUDY OF FIBROMUSCULAR DYSPLASIA REVEALS MECHANISTIC LINKS WITH BLOOD PRESSURE REGULATION AND OTHER VASCULAR DISEASES. (January 2023) Authors: Georges, Adrien; Yang, Min Lee; Berrandou, Takiy Eddine; Liu, Lu; Sayed, Ines Sadoug; Dikilitas, Ozan; Vikkula, Mikka; Januszewicz, Andrzej; Kullo, Iftikhar J; Azizi, Michel; Jeunemaitre, Xavier; Persu, Alexandre; Kovacic, Jason C; Ganesh, Santhi K; Naji, Nabila Bouatia Journal: Journal of hypertension Issue: Volume 41(2023)Supplement 1 Page Start: e54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗