Jeremy Pomeroy to Bardet-Biedl Syndrome
This is a "connection" page, showing publications Jeremy Pomeroy has written about Bardet-Biedl Syndrome.
Connection Strength
4.082
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Pomeroy J, Okorie U, Richardson JG, Faucher A, Ionescu-Ittu R, Vekeman F, Huber C, Haws RM. Clinical burden of hyperphagia, obesity and health outcomes in paediatric individuals with Bardet-Biedl syndrome: A CRIBBS data analysis. Pediatr Obes. 2025 Sep; 20(9):e70026.
Score: 0.913
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Pomeroy J, Offenwanger KM, Timmler T. Diabetes mellitus in Bardet Biedl syndrome. Curr Opin Endocrinol Diabetes Obes. 2023 02 01; 30(1):27-31.
Score: 0.769
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Pomeroy J, VanWormer JJ, Meilahn JR, Maki T, Murali HR, Haws RM. Sleep and physical activity patterns in adults and children with Bardet-Biedl syndrome. Orphanet J Rare Dis. 2021 06 14; 16(1):276.
Score: 0.694
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Pomeroy J, Krentz AD, Richardson JG, Berg RL, VanWormer JJ, Haws RM. Bardet-Biedl syndrome: Weight patterns and genetics in a rare obesity syndrome. Pediatr Obes. 2021 02; 16(2):e12703.
Score: 0.652
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Argente J, Haqq AM, Schorfheide JL, Touchot N, Huber C, Wiedemann U, Pomeroy J. Setmelanotide in Bardet-Biedl Syndrome: A 52-Week Comparison of Phase 3 Trial Participants With a Matched Registry Cohort. Obesity (Silver Spring). 2026 Mar; 34(3):579-587.
Score: 0.240
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Shelton K, Dang P, McCorkle C, Mallipaddi P, Hollman N, Pomeroy J, Richards J. Congenital melanocytic nevi in Bardet-Biedl syndrome. Orphanet J Rare Dis. 2025 Aug 28; 20(1):462.
Score: 0.232
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Forsythe E, Mallya UG, Yang M, Huber C, Cala ML, Greatsinger A, Hagopian E, Pomeroy J, Haqq AM. Burden of hyperphagia and obesity in Bardet-Biedl syndrome: a multicountry survey. Orphanet J Rare Dis. 2023 07 07; 18(1):182.
Score: 0.200
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Forsythe E, Mallya UG, Yang M, Huber C, Cala ML, Greatsinger A, Hagopian E, Pomeroy J, Haqq AM. Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study. Orphanet J Rare Dis. 2023 07 07; 18(1):181.
Score: 0.200
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Meyer JR, Krentz AD, Berg RL, Richardson JG, Pomeroy J, Hebbring SJ, Haws RM. Kidney failure in Bardet-Biedl syndrome. Clin Genet. 2022 04; 101(4):429-441.
Score: 0.183