Projects per year
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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
National Institute of Diabetes and Digestive and Kidney Diseases
5/1/23 → 4/30/24
Project: Research project
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Omega-3 Fatty Acids: Opportunities as Aging Countermeasures
American Federation for Aging Research
1/1/11 → …
Project: Research project
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Mayo Clinic Undiagnosed Disease Network Metabolomics Core
National Center for Advancing Translational Sciences
8/1/18 → 6/30/23
Project: Research project
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Mayo Clinic Physical Activity Research Center: Metabolomics and Proteomics Analysis Site
Nair, K. S. K. S. & Lanza, I. R.
12/8/16 → 11/30/22
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
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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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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 -
EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder
Undiagnosed Diseases Network, 2024, (Accepted/In press) In: American Journal of Medical Genetics, Part A.Research output: Contribution to journal › Article › peer-review