Muenke M - Search Results

1

Cohesin complex-associated holoprosencephaly.

Kruszka P, Berger SI, Casa V, Dekker MR, Gaesser J, Weiss K, Martinez AF, Murdock DR, Louie RJ, Prijoles EJ, Lichty AW, Brouwer OF, Zonneveld-Huijssoon E, Stephan MJ, Hogue J, Hu P, Tanima-Nagai M, Everson JL, Prasad C, Cereda A, Iascone M, Schreiber A, Zurcher V, Corsten-Janssen N, Escobar L, Clegg NJ, Delgado MR, Hajirnis O, Balasubramanian M, Kayserili H, Deardorff M, Poot RA, Wendt KS, Lipinski RJ, Muenke M. Kruszka P, et al. Among authors: muenke m. Brain. 2019 Sep 1;142(9):2631-2643. doi: 10.1093/brain/awz210. Brain. 2019. PMID: 31334757 Free PMC article.

2

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.

Muenke M, Gurrieri F, Bay C, Yi DH, Collins AL, Johnson VP, Hennekam RC, Schaefer GB, Weik L, Lubinsky MS, et al. Muenke M, et al. Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8102-6. doi: 10.1073/pnas.91.17.8102. Proc Natl Acad Sci U S A. 1994. PMID: 8058764 Free PMC article.

3

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.

Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui LC, Muenke M. Roessler E, et al. Among authors: muenke m. Nat Genet. 1996 Nov;14(3):357-60. doi: 10.1038/ng1196-357. Nat Genet. 1996. PMID: 8896572

4

Holoprosencephaly: from Homer to Hedgehog.

Ming JE, Muenke M. Ming JE, et al. Among authors: muenke m. Clin Genet. 1998 Mar;53(3):155-63. doi: 10.1111/j.1399-0004.1998.tb02666.x. Clin Genet. 1998. PMID: 9630065 Review.

5

Holoprosencephaly: a paradigm for the complex genetics of brain development.

Roessler E, Muenke M. Roessler E, et al. Among authors: muenke m. J Inherit Metab Dis. 1998 Aug;21(5):481-97. doi: 10.1023/a:1005406719292. J Inherit Metab Dis. 1998. PMID: 9728329 Review.

6

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.

Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Wallis DE, et al. Among authors: muenke m. Nat Genet. 1999 Jun;22(2):196-8. doi: 10.1038/9718. Nat Genet. 1999. PMID: 10369266

7

Molecular mechanisms of holoprosencephaly.

Wallis DE, Muenke M. Wallis DE, et al. Among authors: muenke m. Mol Genet Metab. 1999 Oct;68(2):126-38. doi: 10.1006/mgme.1999.2895. Mol Genet Metab. 1999. PMID: 10527664 Free article. Review.

8

The molecular genetics of holoprosencephaly: a model of brain development for the next century.

Roessler E, Muenke M. Roessler E, et al. Among authors: muenke m. Childs Nerv Syst. 1999 Nov;15(11-12):646-51. doi: 10.1007/s003810050453. Childs Nerv Syst. 1999. PMID: 10603005 Review.

9

Holoprosencephaly: molecular study of a California population.

Nanni L, Croen LA, Lammer EJ, Muenke M. Nanni L, et al. Among authors: muenke m. Am J Med Genet. 2000 Feb 14;90(4):315-9. doi: 10.1002/(sici)1096-8628(20000214)90:4<315::aid-ajmg10>3.0.co;2-y. Am J Med Genet. 2000. PMID: 10710230

10

Genetics of ventral forebrain development and holoprosencephaly.

Muenke M, Beachy PA. Muenke M, et al. Curr Opin Genet Dev. 2000 Jun;10(3):262-9. doi: 10.1016/s0959-437x(00)00084-8. Curr Opin Genet Dev. 2000. PMID: 10826992 Review.

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