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You searched for: Author/Creator Pollin, Toni I.

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1. Biallelic truncating variants in the muscular A‐type lamin‐interacting protein (MLIP) gene cause myopathy with hyperCKemia. (7th January 2022)

2. Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program. (December 2016)

3. Effects of APOC3 Heterozygous Deficiency on Plasma Lipid and Lipoprotein Metabolism. Issue 1 (January 2019)

4. Enrollment of underrepresented racial and ethnic groups in the Rare and Atypical Diabetes Network (RADIANT). Issue 1 (23rd January 2023)

6. Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels. (9th January 2015)

8. Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an APOC3 Founder Mutation. (December 2017)

9. IGNITE network: Response of patients to genomic medicine interventions. Issue 5 (20th March 2019)

10. Impact of parental relatedness on reproductive outcomes among the Old Order Amish of Lancaster County. Issue 7 (20th April 2022)