U01 HG004599/HG/NHGRI NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
2009	2
2010	11
2011	14
2012	10
2013	13
2014	9
2015	7
2016	8
2017	10
2018	5
2019	4
2020	1
2021	5
2022	0

1

Leeper NJ, Kullo IJ, Cooke JP. Leeper NJ, et al. Circulation. 2012 Jun 26;125(25):3220-8. doi: 10.1161/CIRCULATIONAHA.111.033878. Circulation. 2012. PMID: 22733336 Free PMC article. Review. No abstract available.

2

My Approach to the Patient With Familial Hypercholesterolemia.

Safarova MS, Kullo IJ. Safarova MS, et al. Mayo Clin Proc. 2016 Jun;91(6):770-86. doi: 10.1016/j.mayocp.2016.04.013. Mayo Clin Proc. 2016. PMID: 27261867 Free PMC article. Review.

3

eMERGEing progress in genomics-the first seven years.

Crawford DC, Crosslin DR, Tromp G, Kullo IJ, Kuivaniemi H, Hayes MG, Denny JC, Bush WS, Haines JL, Roden DM, McCarty CA, Jarvik GP, Ritchie MD. Crawford DC, et al. Front Genet. 2014 Jun 17;5:184. doi: 10.3389/fgene.2014.00184. eCollection 2014. Front Genet. 2014. PMID: 24987407 Free PMC article. Review.

4

How rare and common risk variation jointly affect liability for autism spectrum disorder.

Klei L, McClain LL, Mahjani B, Panayidou K, De Rubeis S, Grahnat AS, Karlsson G, Lu Y, Melhem N, Xu X, Reichenberg A, Sandin S, Hultman CM, Buxbaum JD, Roeder K, Devlin B. Klei L, et al. Mol Autism. 2021 Oct 6;12(1):66. doi: 10.1186/s13229-021-00466-2. Mol Autism. 2021. PMID: 34615521 Free PMC article.

5

Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome Phenotypes.

Muhammad A, Aka IT, Birdwell KA, Gordon AS, Roden DM, Wei WQ, Mosley JD, Van Driest SL. Muhammad A, et al. Clin Pharmacol Ther. 2021 Sep;110(3):714-722. doi: 10.1002/cpt.2323. Epub 2021 Jul 12. Clin Pharmacol Ther. 2021. PMID: 34151428

6

Experiences of Latino Participants Receiving Neutral Genomic Screening Results: A Qualitative Study.

Cheema AW, Sutton EJ, Beck AT, Cuellar I, Moreno Garzon GG, Hernandez V, Lindor NM, Shaibi GQ, Kullo IJ, Sharp RR. Cheema AW, et al. Public Health Genomics. 2021 Feb 16;24(1-2):44-53. doi: 10.1159/000513219. Online ahead of print. Public Health Genomics. 2021. PMID: 33592611 Free article.

7

Early identification of cardiovascular risk using genomics and proteomics.

Kullo IJ, Cooper LT. Kullo IJ, et al. Nat Rev Cardiol. 2010 Jun;7(6):309-17. doi: 10.1038/nrcardio.2010.53. Epub 2010 May 4. Nat Rev Cardiol. 2010. PMID: 20440292 Free PMC article. Review.

8

The emerging role of electronic medical records in pharmacogenomics.

Wilke RA, Xu H, Denny JC, Roden DM, Krauss RM, McCarty CA, Davis RL, Skaar T, Lamba J, Savova G. Wilke RA, et al. Clin Pharmacol Ther. 2011 Mar;89(3):379-86. doi: 10.1038/clpt.2010.260. Epub 2011 Jan 19. Clin Pharmacol Ther. 2011. PMID: 21248726 Free PMC article. Review.

9

Genome-wide association studies for atherosclerotic vascular disease and its risk factors.

Ding K, Kullo IJ. Ding K, et al. Circ Cardiovasc Genet. 2009 Feb;2(1):63-72. doi: 10.1161/CIRCGENETICS.108.816751. Circ Cardiovasc Genet. 2009. PMID: 19750184 Free PMC article. Review. No abstract available.

10

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.

Gottesman O, Kuivaniemi H, Tromp G, Faucett WA, Li R, Manolio TA, Sanderson SC, Kannry J, Zinberg R, Basford MA, Brilliant M, Carey DJ, Chisholm RL, Chute CG, Connolly JJ, Crosslin D, Denny JC, Gallego CJ, Haines JL, Hakonarson H, Harley J, Jarvik GP, Kohane I, Kullo IJ, Larson EB, McCarty C, Ritchie MD, Roden DM, Smith ME, Böttinger EP, Williams MS; eMERGE Network. Gottesman O, et al. Genet Med. 2013 Oct;15(10):761-71. doi: 10.1038/gim.2013.72. Epub 2013 Jun 6. Genet Med. 2013. PMID: 23743551 Free PMC article. Review.

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