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Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
Audain E, Wilsdon A, Breckpot J, Izarzugaza JMG, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson DW, Berger F, Daehnert I, Devriendt K, Dittrich S, Daubeney PE, Garg V, Hackmann K, Hoff K, Hofmann P, Dombrowsky G, Pickardt T, Bauer U, Keavney BD, Klaassen S, Kramer HH, Marshall CR, Milewicz DM, Lemaire S, Coselli JS, Mitchell ME, Tomita-Mitchell A, Prakash SK, Stamm K, Stewart AFR, Silversides CK, Siebert R, Stiller B, Rosenfeld JA, Vater I, Postma AV, Caliebe A, Brook JD, Andelfinger G, Hurles ME, Thienpont B, Larsen LA, Hitz MP. Audain E, et al. Among authors: mitchell me. PLoS Genet. 2021 Sep 21;17(9):e1009809. doi: 10.1371/journal.pgen.1009809. eCollection 2021 Sep. PLoS Genet. 2021. PMID: 34547032 Free PMC article.
Molecular and cellular basis of congenital heart disease.
Sander TL, Klinkner DB, Tomita-Mitchell A, Mitchell ME. Sander TL, et al. Among authors: mitchell me. Pediatr Clin North Am. 2006 Oct;53(5):989-1009, x. doi: 10.1016/j.pcl.2006.08.010. Pediatr Clin North Am. 2006. PMID: 17027620 Review.
The molecular basis of congenital heart disease.
Mitchell ME, Sander TL, Klinkner DB, Tomita-Mitchell A. Mitchell ME, et al. Semin Thorac Cardiovasc Surg. 2007 Fall;19(3):228-37. doi: 10.1053/j.semtcvs.2007.07.013. Semin Thorac Cardiovasc Surg. 2007. PMID: 17983950 Review.
Investigation of somatic NKX2-5 mutations in congenital heart disease.
Draus JM Jr, Hauck MA, Goetsch M, Austin EH 3rd, Tomita-Mitchell A, Mitchell ME. Draus JM Jr, et al. Among authors: mitchell me. J Med Genet. 2009 Feb;46(2):115-22. doi: 10.1136/jmg.2008.060277. J Med Genet. 2009. PMID: 19181906 Free PMC article.
Impact of MYH6 variants in hypoplastic left heart syndrome.
Tomita-Mitchell A, Stamm KD, Mahnke DK, Kim MS, Hidestrand PM, Liang HL, Goetsch MA, Hidestrand M, Simpson P, Pelech AN, Tweddell JS, Benson DW, Lough JW, Mitchell ME. Tomita-Mitchell A, et al. Among authors: mitchell me. Physiol Genomics. 2016 Dec 1;48(12):912-921. doi: 10.1152/physiolgenomics.00091.2016. Epub 2016 Oct 27. Physiol Genomics. 2016. PMID: 27789736 Free PMC article.
Effect of endomyocardial biopsy on levels of donor-specific cell-free DNA.
Zangwill SD, Stamm KD, Hidestrand M, Tomita-Mitchell A, Mitchell ME. Zangwill SD, et al. Among authors: mitchell me. J Heart Lung Transplant. 2019 Oct;38(10):1118-1120. doi: 10.1016/j.healun.2019.06.005. Epub 2019 Jun 28. J Heart Lung Transplant. 2019. PMID: 31324442 Free PMC article. No abstract available.
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
Audain E, Wilsdon A, Breckpot J, Izarzugaza JMG, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson DW, Berger F, Daehnert I, Devriendt K, Dittrich S, Daubeney PE, Garg V, Hackmann K, Hoff K, Hofmann P, Dombrowsky G, Pickardt T, Bauer U, Keavney BD, Klaassen S, Kramer HH, Marshall CR, Milewicz DM, Lemaire S, Coselli JS, Mitchell ME, Tomita-Mitchell A, Prakash SK, Stamm K, Stewart AFR, Silversides CK, Siebert R, Stiller B, Rosenfeld JA, Vater I, Postma AV, Caliebe A, Brook JD, Andelfinger G, Hurles ME, Thienpont B, Larsen LA, Hitz MP. Audain E, et al. Among authors: mitchell me. PLoS Genet. 2021 Jul 29;17(7):e1009679. doi: 10.1371/journal.pgen.1009679. eCollection 2021 Jul. PLoS Genet. 2021. PMID: 34324492 Free PMC article.
Human gene copy number spectra analysis in congenital heart malformations.
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME. Tomita-Mitchell A, et al. Among authors: mitchell me. Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7. Physiol Genomics. 2012. PMID: 22318994 Free PMC article.
387 results