| Year |
Citation |
Score |
| 2012 |
Solomon BD, Bear KA, Wyllie A, Keaton AA, Dubourg C, David V, Mercier S, Odent S, Hehr U, Paulussen A, Clegg NJ, Delgado MR, Bale SJ, Lacbawan F, Ardinger HH, et al. Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. Journal of Medical Genetics. 49: 473-9. PMID 22791840 DOI: 10.1136/jmedgenet-2012-101008 |
0.522 |
|
| 2011 |
Wannasilp N, Solomon BD, Warren-Mora N, Clegg NJ, Delgado MR, Lacbawan F, Hu P, Winder TL, Roessler E, Muenke M. Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2. American Journal of Medical Genetics. Part A. 155: 860-4. PMID 21416594 DOI: 10.1002/ajmg.a.33903 |
0.352 |
|
| 2010 |
Keaton AA, Solomon BD, Kauvar EF, El-Jaick KB, Gropman AL, Zafer Y, Meck JM, Bale SJ, Grange DK, Haddad BR, Gowans GC, Clegg NJ, Delgado MR, Hahn JS, Pineda-Alvarez DE, et al. TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype. Molecular Syndromology. 1: 211-222. PMID 22125506 DOI: 10.1159/000328203 |
0.326 |
|
| 2010 |
Solomon BD, Lacbawan F, Mercier S, Clegg NJ, Delgado MR, Rosenbaum K, Dubourg C, David V, Olney AH, Wehner LE, Hehr U, Bale S, Paulussen A, Smeets HJ, Hardisty E, et al. Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. Journal of Medical Genetics. 47: 513-24. PMID 19955556 DOI: 10.1136/Jmg.2009.073049 |
0.471 |
|
| 2009 |
Lacbawan F, Solomon BD, Roessler E, El-Jaick K, Domené S, Vélez JI, Zhou N, Hadley D, Balog JZ, Long R, Fryer A, Smith W, Omar S, McLean SD, Clarkson K, ... ... Clegg NJ, et al. Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. Journal of Medical Genetics. 46: 389-98. PMID 19346217 DOI: 10.1136/Jmg.2008.063818 |
0.426 |
|
| 2003 |
Findley SD, Tamanaha M, Clegg NJ, Ruohola-Baker H. Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage. Development (Cambridge, England). 130: 859-71. PMID 12538514 DOI: 10.1242/Dev.00310 |
0.362 |
|
| 1998 |
Clegg NJ, Honda BM, Whitehead IP, Grigliatti TA, Wakimoto B, Brock HW, Lloyd VK, Sinclair DA. Suppressors of position-effect variegation in Drosophila melanogaster affect expression of the heterochromatic gene light in the absence of a chromosome rearrangement. Genome / National Research Council Canada = Gã©Nome / Conseil National De Recherches Canada. 41: 495-503. PMID 9796098 DOI: 10.1139/G98-041 |
0.673 |
|
| 1998 |
Sinclair DA, Clegg NJ, Antonchuk J, Milne TA, Stankunas K, Ruse C, Grigliatti TA, Kassis JA, Brock HW. Enhancer of Polycomb is a suppressor of position-effect variegation in Drosophila melanogaster. Genetics. 148: 211-20. PMID 9475733 |
0.663 |
|
| 1993 |
Clegg NJ, Whitehead IP, Brock JK, Sinclair DA, Mottus R, Stromotich G, Harrington MJ, Grigliatti TA. A cytogenetic analysis of chromosomal region 31 of Drosophila melanogaster. Genetics. 134: 221-30. PMID 8514131 |
0.595 |
|
| 1993 |
Clegg NJ, Whitehead IP, Williams JA, Spiegelman GB, Grigliatti TA. A developmental and molecular analysis of Cdc2 mutations in Drosophila melanogaster. Genome / National Research Council Canada = GéNome / Conseil National De Recherches Canada. 36: 676-85. PMID 8405984 DOI: 10.1139/G93-091 |
0.685 |
|
| 1993 |
Stern B, Ried G, Clegg NJ, Grigliatti TA, Lehner CF. Genetic analysis of the Drosophila cdc2 homolog. Development (Cambridge, England). 117: 219-32. PMID 8223248 |
0.647 |
|
| 1992 |
Sinclair DA, Ruddell AA, Brock JK, Clegg NJ, Lloyd VK, Grigliatti TA. A cytogenetic and genetic characterization of a group of closely linked second chromosome mutations that suppress position-effect variegation in Drosophila melanogaster. Genetics. 130: 333-44. PMID 1541393 |
0.705 |
|
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