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Mutations in sphingolipid metabolism genes are associated with ADHD.
Henriquez-Henriquez M, Acosta MT, Martinez AF, Vélez JI, Lopera F, Pineda D, Palacio JD, Quiroga T, Worgall TS, Deckelbaum RJ, Mastronardi C, Molina BSG; MTA Cooperative Group; Arcos-Burgos M, Muenke M. Henriquez-Henriquez M, et al. Among authors: muenke m. Transl Psychiatry. 2020 Jul 13;10(1):231. doi: 10.1038/s41398-020-00881-8. Transl Psychiatry. 2020. PMID: 32661301 Free PMC article.
Genetics of population isolates.
Arcos-Burgos M, Muenke M. Arcos-Burgos M, et al. Among authors: muenke m. Clin Genet. 2002 Apr;61(4):233-47. doi: 10.1034/j.1399-0004.2002.610401.x. Clin Genet. 2002. PMID: 12030885 Review.
Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families.
Palacio JD, Castellanos FX, Pineda DA, Lopera F, Arcos-Burgos M, Quiroz YT, Henao GC, Puerta IC, Ramírez DL, Rapoport JL, Bailey-Wilson J, Berg K, Muenke M. Palacio JD, et al. Among authors: muenke m. J Am Acad Child Adolesc Psychiatry. 2004 Dec;43(12):1506-15. doi: 10.1097/01.chi.0000142279.79805.dc. J Am Acad Child Adolesc Psychiatry. 2004. PMID: 15564820
Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci.
Jain M, Palacio LG, Castellanos FX, Palacio JD, Pineda D, Restrepo MI, Muñoz JF, Lopera F, Wallis D, Berg K, Bailey-Wilson JE, Arcos-Burgos M, Muenke M. Jain M, et al. Among authors: muenke m. Biol Psychiatry. 2007 Jun 15;61(12):1329-39. doi: 10.1016/j.biopsych.2006.06.026. Epub 2006 Sep 1. Biol Psychiatry. 2007. PMID: 16950213
Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions.
Acosta MT, Castellanos FX, Bolton KL, Balog JZ, Eagen P, Nee L, Jones J, Palacio L, Sarampote C, Russell HF, Berg K, Arcos-Burgos M, Muenke M. Acosta MT, et al. Among authors: muenke m. J Am Acad Child Adolesc Psychiatry. 2008 Jul;47(7):797-807. doi: 10.1097/CHI.0b013e318173f70b. J Am Acad Child Adolesc Psychiatry. 2008. PMID: 18520958 Free PMC article.
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
Roessler E, Ouspenskaia MV, Karkera JD, Vélez JI, Kantipong A, Lacbawan F, Bowers P, Belmont JW, Towbin JA, Goldmuntz E, Feldman B, Muenke M. Roessler E, et al. Among authors: muenke m. Am J Hum Genet. 2008 Jul;83(1):18-29. doi: 10.1016/j.ajhg.2008.05.012. Epub 2008 Jun 5. Am J Hum Genet. 2008. PMID: 18538293 Free PMC article.
324 results