Cooper ME - Search Results

1

Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome.

Weese-Mayer DE, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Maher BS, Cooper ME, Marazita ML. Weese-Mayer DE, et al. Among authors: cooper me. Am J Med Genet. 2001 May 1;100(3):237-45. doi: 10.1002/ajmg.1249. Am J Med Genet. 2001. PMID: 11343310

2

Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome.

Marazita ML, Maher BS, Cooper ME, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Weese-Mayer DE. Marazita ML, et al. Among authors: cooper me. Am J Med Genet. 2001 May 1;100(3):229-36. doi: 10.1002/ajmg.1284. Am J Med Genet. 2001. PMID: 11343309

3

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.

Rand CM, Weese-Mayer DE, Zhou L, Maher BS, Cooper ME, Marazita ML, Berry-Kravis EM. Rand CM, et al. Among authors: cooper me. Am J Med Genet A. 2006 Aug 1;140(15):1687-91. doi: 10.1002/ajmg.a.31336. Am J Med Genet A. 2006. PMID: 16830328 No abstract available.

4

Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate.

Neiswanger K, Walker K, Klotz CM, Cooper ME, Bardi KM, Brandon CA, Weinberg SM, Vieira AR, Martin RA, Czeizel AE, Castilla EE, Poletta FA, Marazita ML. Neiswanger K, et al. Among authors: cooper me. Am J Med Genet A. 2009 Dec;149A(12):2673-9. doi: 10.1002/ajmg.a.33089. Am J Med Genet A. 2009. PMID: 19921634 Free PMC article.

5

Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate.

Neiswanger K, Weinberg SM, Rogers CR, Brandon CA, Cooper ME, Bardi KM, Deleyiannis FW, Resick JM, Bowen A, Mooney MP, de Salamanca JE, González B, Maher BS, Martin RA, Marazita ML. Neiswanger K, et al. Among authors: cooper me. Am J Med Genet A. 2007 Jun 1;143A(11):1143-9. doi: 10.1002/ajmg.a.31760. Am J Med Genet A. 2007. PMID: 17497721

6

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families.

Schultz RE, Cooper ME, Daack-Hirsch S, Shi M, Nepomucena B, Graf KA, O'Brien EK, O'Brien SE, Marazita ML, Murray JC. Schultz RE, et al. Among authors: cooper me. Am J Med Genet A. 2004 Feb 15;125A(1):17-22. doi: 10.1002/ajmg.a.20424. Am J Med Genet A. 2004. PMID: 14755461

7

A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23.

Riley BM, Schultz RE, Cooper ME, Goldstein-McHenry T, Daack-Hirsch S, Lee KT, Dragan E, Vieira AR, Lidral AC, Marazita ML, Murray JC. Riley BM, et al. Among authors: cooper me. Am J Med Genet A. 2007 Apr 15;143A(8):846-52. doi: 10.1002/ajmg.a.31673. Am J Med Genet A. 2007. PMID: 17366557 Free PMC article.

8

Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).

Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC. Butali A, et al. Among authors: cooper me. Am J Med Genet A. 2013 May;161A(5):965-72. doi: 10.1002/ajmg.a.35749. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463464 Free PMC article.

9

Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.

Leslie EJ, Mancuso JL, Schutte BC, Cooper ME, Durda KM, L'Heureux J, Zucchero TM, Marazita ML, Murray JC. Leslie EJ, et al. Among authors: cooper me. Am J Med Genet A. 2013 Oct;161A(10):2535-2544. doi: 10.1002/ajmg.a.36133. Epub 2013 Aug 15. Am J Med Genet A. 2013. PMID: 23949966 Free PMC article.

10

Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey.

Marazita ML, Field LL, Tunçbilek G, Cooper ME, Goldstein T, Gürsu KG. Marazita ML, et al. Among authors: cooper me. Am J Med Genet A. 2004 Apr 15;126A(2):111-22. doi: 10.1002/ajmg.a.20564. Am J Med Genet A. 2004. PMID: 15057975

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