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Association of the DTNBP1 locus with schizophrenia in a U.S. population.
Funke B, Finn CT, Plocik AM, Lake S, DeRosse P, Kane JM, Kucherlapati R, Malhotra AK. Funke B, et al. Among authors: kucherlapati r. Am J Hum Genet. 2004 Nov;75(5):891-8. doi: 10.1086/425279. Epub 2004 Sep 10. Am J Hum Genet. 2004. PMID: 15362017 Free PMC article.
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Chen PC, Yin J, Yu HW, Yuan T, Fernandez M, Yung CK, Trinh QM, Peltekova VD, Reid JG, Tworog-Dube E, Morgan MB, Muzny DM, Stein L, McPherson JD, Roberts AE, Gibbs RA, Neel BG, Kucherlapati R. Chen PC, et al. Among authors: kucherlapati r. Proc Natl Acad Sci U S A. 2014 Aug 5;111(31):11473-8. doi: 10.1073/pnas.1324128111. Epub 2014 Jul 21. Proc Natl Acad Sci U S A. 2014. PMID: 25049390 Free PMC article.
Genetic variation in DTNBP1 influences general cognitive ability.
Burdick KE, Lencz T, Funke B, Finn CT, Szeszko PR, Kane JM, Kucherlapati R, Malhotra AK. Burdick KE, et al. Among authors: kucherlapati r. Hum Mol Genet. 2006 May 15;15(10):1563-8. doi: 10.1093/hmg/ddi481. Epub 2006 Jan 13. Hum Mol Genet. 2006. PMID: 16415041
Shared genetic causes of cardiac hypertrophy in children and adults.
Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE. Morita H, et al. Among authors: kucherlapati r. N Engl J Med. 2008 May 1;358(18):1899-908. doi: 10.1056/NEJMoa075463. Epub 2008 Apr 9. N Engl J Med. 2008. PMID: 18403758 Free PMC article.
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.
Lencz T, Lambert C, DeRosse P, Burdick KE, Morgan TV, Kane JM, Kucherlapati R, Malhotra AK. Lencz T, et al. Among authors: kucherlapati r. Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):19942-7. doi: 10.1073/pnas.0710021104. Epub 2007 Dec 5. Proc Natl Acad Sci U S A. 2007. PMID: 18077426 Free PMC article.
394 results