Carrasquillo MM - Search Results

1

Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins.

Oatman SR, Reddy JS, Quicksall Z, Carrasquillo MM, Wang X, Liu CC, Yamazaki Y, Nguyen TT, Malphrus K, Heckman M, Biswas K, Nho K, Baker M, Martens YA, Zhao N, Kim JP, Risacher SL, Rademakers R, Saykin AJ, DeTure M, Murray ME, Kanekiyo T; Alzheimer’s Disease Neuroimaging Initiative; Dickson DW, Bu G, Allen M, Ertekin-Taner N. Oatman SR, et al. Among authors: carrasquillo mm. Mol Neurodegener. 2023 Jan 7;18(1):2. doi: 10.1186/s13024-022-00592-2. Mol Neurodegener. 2023. PMID: 36609403 Free PMC article.

2

Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.

Shaw SH, Carrasquillo MM, Kashuk C, Puffenberger EG, Chakravarti A. Shaw SH, et al. Among authors: carrasquillo mm. Genome Res. 1998 Feb;8(2):111-23. doi: 10.1101/gr.8.2.111. Genome Res. 1998. PMID: 9477339 Free article.

3

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

Carrasquillo MM, Zlotogora J, Barges S, Chakravarti A. Carrasquillo MM, et al. Hum Mol Genet. 1997 Nov;6(12):2163-72. doi: 10.1093/hmg/6.12.2163. Hum Mol Genet. 1997. PMID: 9328482

4

High-throughput variation detection and genotyping using microarrays.

Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A. Cutler DJ, et al. Among authors: carrasquillo mm. Genome Res. 2001 Nov;11(11):1913-25. doi: 10.1101/gr.197201. Genome Res. 2001. PMID: 11691856 Free PMC article.

5

Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.

Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Saleh B, Pratt H. Engel-Yeger B, et al. Hear Res. 2003 Jan;175(1-2):140-51. doi: 10.1016/s0378-5955(02)00719-0. Hear Res. 2003. PMID: 12527132

6

Genomic variation in multigenic traits: Hirschsprung disease.

McCallion AS, Emison ES, Kashuk CS, Bush RT, Kenton M, Carrasquillo MM, Jones KW, Kennedy GC, Portnoy ME, Green ED, Chakravarti A. McCallion AS, et al. Among authors: carrasquillo mm. Cold Spring Harb Symp Quant Biol. 2003;68:373-81. doi: 10.1101/sqb.2003.68.373. Cold Spring Harb Symp Quant Biol. 2003. PMID: 15338639 No abstract available.

7

Postnatal downregulation of inhibitory neuromuscular transmission to the longitudinal muscle of the guinea pig ileum.

Bian X, Burda JE, Carrasquillo M, Galligan JJ. Bian X, et al. Neurogastroenterol Motil. 2009 Sep;21(9):969-77. doi: 10.1111/j.1365-2982.2009.01296.x. Epub 2009 Apr 17. Neurogastroenterol Motil. 2009. PMID: 19374637

8

Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.

Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A. Carrasquillo MM, et al. Nat Genet. 2002 Oct;32(2):237-44. doi: 10.1038/ng998. Epub 2002 Sep 23. Nat Genet. 2002. PMID: 12355085

9

The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.

Engel-Yeger B, Zaaroura S, Zlotogora J, Shalev S, Hujeirat Y, Carrasquillo M, Barges S, Pratt H. Engel-Yeger B, et al. Hear Res. 2002 Jan;163(1-2):93-100. doi: 10.1016/s0378-5955(01)00386-0. Hear Res. 2002. PMID: 11788203

10

Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids.

Harte PJ, Wu W, Carrasquillo MM, Matera AG. Harte PJ, et al. Among authors: carrasquillo mm. Cytogenet Cell Genet. 1999;84(1-2):83-6. doi: 10.1159/000015220. Cytogenet Cell Genet. 1999. PMID: 10343109

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