| 1 | Intermittent fasting strategies for metabolic dysfunction-associated steatotic liver disease: A systematic review and frequentist network meta-analysis of randomized controlled trials. (Abu Suilik H, Farid Gadelmawla A, Rifai M, Alhawi M, Ashour A, Abdalshafy H, Abdullah Bataineh O, Rezq H, Bani Hani A, Elkhattib I, Abuelazm M) Clin Nutr ESPEN 2026 Oct;75:103415 |
| 1 | Walking the VLDL tightrope in cardiometabolic diseases. (Kim M, Zheng Z) Trends Endocrinol Metab 2025 Mar;36(3):278-291 4 Citations |
| 1 | Metabolic Bariatric Surgery Across the IFSO Chapters: Key Insights on the Baseline Patient Demographics, Procedure Types, and Mortality from the Eighth IFSO Global Registry Report. (Brown WA, Liem R, Al-Sabah S, Anvari M, Boza C, Cohen RV, Ghaferi A, Våge V, Himpens J, Kow L, Morton J, Musella M, Pattou F, Sakran N, Clapp B, Prager G, Shikora S, IFSO Global Registry Collaboration) Obes Surg 2024 May;34(5):1764-1777 134 Citations |
| 2 | Inherited monogenic defects of ceramide metabolism: Molecular bases and diagnoses. (Dubot P, Sabourdy F, Rybova J, Medin JA, Levade T) Clin Chim Acta 2019 Aug;495:457-466 4 Citations |
| 1 | Discovery of Novel Pyruvate Dehydrogenase Kinase 4 Inhibitors for Potential Oral Treatment of Metabolic Diseases. (Lee D, Pagire HS, Pagire SH, Bae EJ, Dighe M, Kim M, Lee KM, Jang YK, Jaladi AK, Jung KY, Yoo EK, Gim HE, Lee S, Choi WI, Chi YI, Song JS, Bae MA, Jeon YH, Lee GH, Liu KH, Lee T, Park S, Jeon JH, Lee IK, Ahn JH) J Med Chem 2019 Jan 24;62(2):575-588 24 Citations |
| 1 | The Hematopoietic Cell Transplant Comorbidity Index predicts survival after allogeneic transplant for nonmalignant diseases. (Thakar MS, Broglie L, Logan B, Artz A, Bunin N, Burroughs LM, Fretham C, Jacobsohn DA, Loren AW, Kurtzberg J, Martinez CA, Mineishi S, Nelson AS, Woolfrey A, Pasquini MC, Sorror ML) Blood 2019 Feb 14;133(7):754-762 60 Citations |
| 1 | Short telomere syndromes cause a primary T cell immunodeficiency. (Wagner CL, Hanumanthu VS, Talbot CC Jr, Abraham RS, Hamm D, Gable DL, Kanakry CG, Applegate CD, Siliciano J, Jackson JB, Desiderio S, Alder JK, Luznik L, Armanios M) J Clin Invest 2018 Dec 03;128(12):5222-5234 112 Citations |
| 1 | The Modern Metabolic Stone Evaluation in Children. (Bevill M, Kattula A, Cooper CS, Storm DW) Urology 2017 Mar;101:15-20 33 Citations |
| 2 | Adiponectin Levels Differentiate Metabolically Healthy vs Unhealthy Among Obese and Nonobese White Individuals. (Ahl S, Guenther M, Zhao S, James R, Marks J, Szabo A, Kidambi S) J Clin Endocrinol Metab 2015 Nov;100(11):4172-80 112 Citations |
| 2 | Sequence-specific recruitment of heterochromatin protein 1 via interaction with Krüppel-like factor 11, a human transcription factor involved in tumor suppression and metabolic diseases. (Lomberk G, Mathison AJ, Grzenda A, Seo S, DeMars CJ, Ilyas SI, Bonilla-Velez J, Calvo E, Fernandez-Zapico ME, Iovanna J, Buttar NS, Urrutia R) J Biol Chem 2012 Apr 13;287(16):13026-39 48 Citations |
| 3 | BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome. (Reis LM, Tyler RC, Schilter KF, Abdul-Rahman O, Innis JW, Kozel BA, Schneider AS, Bardakjian TM, Lose EJ, Martin DM, Broeckel U, Semina EV) Hum Genet 2011 Oct;130(4):495-504 102 Citations |
| 1 | RGD: a comparative genomics platform. (Shimoyama M, Smith JR, Hayman T, Laulederkind S, Lowry T, Nigam R, Petri V, Wang SJ, Dwinell M, Jacob H, RGD Team) Hum Genomics 2011 Jan;5(2):124-9 22 Citations |
| 1 | Metabolic myopathies discovered during investigations of statin myopathy. (Baker SK, Vladutiu GD, Peltier WL, Isackson PJ, Tarnopolsky MA) Can J Neurol Sci 2008 Mar;35(1):94-7 27 Citations |
| 2 | The application of microarray analysis to pediatric diseases. (Hessner MJ, Liang M, Kwitek AE) Pediatr Clin North Am 2006 Aug;53(4):579-90 2 Citations |
| 2 | Mapping the genetic determinants of hypertension, metabolic diseases, and related phenotypes in the lyon hypertensive rat. (Bilusic M, Bataillard A, Tschannen MR, Gao L, Barreto NE, Vincent M, Wang T, Jacob HJ, Sassard J, Kwitek AE) Hypertension 2004 Nov;44(5):695-701 50 Citations |
| 1 | A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population. (Gross M, Rötzer E, Kölle P, Mortier W, Reichmann H, Goebel HH, Lochmüller H, Pongratz D, Mahnke-Zizelman DK, Sabina RL) Neuromuscul Disord 2002 Aug;12(6):558-65 34 Citations |
| 1 | The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. (Comuzzie AG, Funahashi T, Sonnenberg G, Martin LJ, Jacob HJ, Black AE, Maas D, Takahashi M, Kihara S, Tanaka S, Matsuzawa Y, Blangero J, Cohen D, Kissebah A) J Clin Endocrinol Metab 2001 Sep;86(9):4321-5 290 Citations |
