Heiman M - Search Results

1

A null mutation in SERPINE1 protects against biological aging in humans.

Khan SS, Shah SJ, Klyachko E, Baldridge AS, Eren M, Place AT, Aviv A, Puterman E, Lloyd-Jones DM, Heiman M, Miyata T, Gupta S, Shapiro AD, Vaughan DE. Khan SS, et al. Among authors: heiman m. Sci Adv. 2017 Nov 15;3(11):eaao1617. doi: 10.1126/sciadv.aao1617. eCollection 2017 Nov. Sci Adv. 2017. PMID: 29152572 Free PMC article.

2

Biologic response to subcutaneous and intranasal therapy with desmopressin in a large Amish kindred with Type 2M von Willebrand disease.

Sharthkumar A, Greist A, Di Paola J, Winay J, Roberson C, Heiman M, Herbert S, Parameswaran R, Shapiro A. Sharthkumar A, et al. Among authors: heiman m. Haemophilia. 2008 May;14(3):539-48. doi: 10.1111/j.1365-2516.2008.01666.x. Epub 2008 Feb 25. Haemophilia. 2008. PMID: 18312368

3

Variability in bleeding phenotype in Amish carriers of haemophilia B with the 31008 C-->T mutation.

Sharathkumar A, Hardesty B, Greist A, Salter J, Kerlin B, Heiman M, Sulkin M, Shapiro A. Sharathkumar A, et al. Among authors: heiman m. Haemophilia. 2009 Jan;15(1):91-100. doi: 10.1111/j.1365-2516.2008.01792.x. Epub 2008 Jul 24. Haemophilia. 2009. PMID: 18721150

4

The obstetric, gynaecological and fertility implications of homozygous PAI-1 deficiency: single-centre experience.

Heiman M, Gupta S, Shapiro AD. Heiman M, et al. Haemophilia. 2014 May;20(3):407-12. doi: 10.1111/hae.12313. Epub 2013 Nov 22. Haemophilia. 2014. PMID: 24261743

5

Variable bleeding phenotype in an Amish pedigree with von Willebrand disease.

Gupta S, Heiman M, Duncan N, Hinckley J, Di Paola J, Shapiro AD. Gupta S, et al. Among authors: heiman m. Am J Hematol. 2016 Oct;91(10):E431-5. doi: 10.1002/ajh.24474. Epub 2016 Aug 22. Am J Hematol. 2016. PMID: 27414491 Free PMC article.

6

Mathematical model of thrombin generation and bleeding phenotype in Amish carriers of Factor IX:C deficiency vs. controls.

Gupta S, Bravo MC, Heiman M, Nakar C, Brummel-Ziedins K, Miller CH, Shapiro A. Gupta S, et al. Among authors: heiman m. Thromb Res. 2019 Oct;182:43-50. doi: 10.1016/j.thromres.2019.07.020. Epub 2019 Aug 8. Thromb Res. 2019. PMID: 31446339 Free PMC article.

7

Identification of Cardiac Fibrosis in Young Adults With a Homozygous Frameshift Variant in SERPINE1.

Khan SS, Shah SJ, Strande JL, Baldridge AS, Flevaris P, Puckelwartz MJ, McNally EM, Rasmussen-Torvik LJ, Lee DC, Carr JC, Benefield BC, Afzal MZ, Heiman M, Gupta S, Shapiro AD, Vaughan DE. Khan SS, et al. Among authors: heiman m. JAMA Cardiol. 2021 Jul 1;6(7):841-846. doi: 10.1001/jamacardio.2020.6909. JAMA Cardiol. 2021. PMID: 33439236 Free PMC article.

8

Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits.

Hinckley JD, Abbott D, Burns TL, Heiman M, Shapiro AD, Wang K, Di Paola J. Hinckley JD, et al. Among authors: heiman m. Mol Genet Genomic Med. 2013 Sep 1;1(3):131-141. doi: 10.1002/mgg3.16. Mol Genet Genomic Med. 2013. PMID: 24058921 Free PMC article.

9

A tangled web: Dual diagnosis of hereditary hemorrhagic telangiectasia and familial cerebral cavernous malformation.

Kumar M, Fleck C, Heiman M. Kumar M, et al. Among authors: heiman m. Pediatr Blood Cancer. 2023 Oct;70(10):e30499. doi: 10.1002/pbc.30499. Epub 2023 Jun 19. Pediatr Blood Cancer. 2023. PMID: 37336838 No abstract available.

10

Dendrite morphogenesis in Caenorhabditis elegans.

Heiman MG, Bülow HE. Heiman MG, et al. Genetics. 2024 May 24:iyae056. doi: 10.1093/genetics/iyae056. Online ahead of print. Genetics. 2024. PMID: 38785371

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