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Dive into the research topics where Ian R Lanza is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Exercise Response in Humans with Obesity
Lanza, I. R. (PI)
National Institute of Diabetes and Digestive and Kidney Diseases
5/1/23 → 4/30/25
Project: Research project
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Mayo Clinic Physical Activity Research Center: Metabolomics and Proteomics Analysis Site
Nair, K. S. K. (PI) & Lanza, I. R. (CoPI)
National Institute of Diabetes and Digestive and Kidney Diseases
12/8/16 → 5/31/25
Project: Research project
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Omega-3 Fatty Acids: Opportunities as Aging Countermeasures
Lanza, I. R. (PI)
American Federation for Aging Research
1/1/11 → …
Project: Research project
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Mayo Clinic Undiagnosed Disease Network Metabolomics Core
Lanza, I. R. (PI) & Oglesbee, D. (CoPI)
National Center for Advancing Translational Sciences
8/1/18 → 6/30/23
Project: Research project
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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3
Undiagnosed Diseases Network, Jan 4 2024, In: American journal of human genetics. 111, 1, p. 96-118 23 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Deciphering Developmental Disorders, Genomics England Research Consortium & Undiagnosed Disease Network, Feb 2024, In: Genetics in Medicine. 26, 2, 101023.Research output: Contribution to journal › Article › peer-review
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Cardiac resynchronization therapy for patients with mild to moderately reduced ejection fraction and left bundle branch block
Cha, Y. M., Lee, H. C., Mulpuru, S. K., Deshmukh, A. J., Friedman, P. A., Asirvatham, S. J., Bradley, D. J., Madhavan, M., Abou Ezzeddine, O. F., Wen, S., Liddell, B. W., Curran, C., Li, C., Dasari, S., Lanza, I. R., Bailey, K. R. & Chen, H. H., Nov 2024, In: Heart rhythm. 21, 11, p. 2250-2259 10 p.Research output: Contribution to journal › Article › peer-review
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De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities
Undiagnosed Diseases Network, Jan 2024, In: American Journal of Medical Genetics, Part A. 194, 1, p. 17-30 14 p.Research output: Contribution to journal › Article › peer-review
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De novo variants in DENND5B cause a neurodevelopmental disorder
Undiagnosed Diseases Network, Mar 7 2024, In: American journal of human genetics. 111, 3, p. 529-543 15 p.Research output: Contribution to journal › Article › peer-review
Open Access