Muenke M - Search Results

1

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.

Arcos-Burgos M, Jain M, Acosta MT, Shively S, Stanescu H, Wallis D, Domené S, Vélez JI, Karkera JD, Balog J, Berg K, Kleta R, Gahl WA, Roessler E, Long R, Lie J, Pineda D, Londoño AC, Palacio JD, Arbelaez A, Lopera F, Elia J, Hakonarson H, Johansson S, Knappskog PM, Haavik J, Ribases M, Cormand B, Bayes M, Casas M, Ramos-Quiroga JA, Hervas A, Maher BS, Faraone SV, Seitz C, Freitag CM, Palmason H, Meyer J, Romanos M, Walitza S, Hemminger U, Warnke A, Romanos J, Renner T, Jacob C, Lesch KP, Swanson J, Vortmeyer A, Bailey-Wilson JE, Castellanos FX, Muenke M. Arcos-Burgos M, et al. Among authors: muenke m. Mol Psychiatry. 2010 Nov;15(11):1053-66. doi: 10.1038/mp.2010.6. Epub 2010 Feb 16. Mol Psychiatry. 2010. PMID: 20157310 Free article.

2

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.

Roessler E, Belloni E, Gaudenz K, Vargas F, Scherer SW, Tsui LC, Muenke M. Roessler E, et al. Among authors: muenke m. Hum Mol Genet. 1997 Oct;6(11):1847-53. doi: 10.1093/hmg/6.11.1847. Hum Mol Genet. 1997. PMID: 9302262

3

Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4.

Gaudenz K, Roessler E, Vainikka S, Alitalo K, Muenke M. Gaudenz K, et al. Among authors: muenke m. Mol Genet Metab. 1998 May;64(1):76-9. doi: 10.1006/mgme.1998.2694. Mol Genet Metab. 1998. PMID: 9682222 Free article.

4

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.

5

Human developmental disorders and the Sonic hedgehog pathway.

Ming JE, Roessler E, Muenke M. Ming JE, et al. Among authors: muenke m. Mol Med Today. 1998 Aug;4(8):343-9. doi: 10.1016/s1357-4310(98)01299-4. Mol Med Today. 1998. PMID: 9755453 Review.

6

Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome.

Cornejo-Roldan LR, Roessler E, Muenke M. Cornejo-Roldan LR, et al. Among authors: muenke m. Hum Genet. 1999 May;104(5):425-31. doi: 10.1007/s004390050979. Hum Genet. 1999. PMID: 10394936

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

Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).

Roessler E, Mittaz L, Du Y, Scott HS, Chang J, Rossier C, Guipponi M, Matsuda SP, Muenke M, Antonarakis SE. Roessler E, et al. Among authors: muenke m. Hum Genet. 1999 Nov;105(5):489-95. doi: 10.1007/s004390051135. Hum Genet. 1999. PMID: 10598817

9

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.

10

Mutations in holoprosencephaly.

Wallis D, Muenke M. Wallis D, et al. Among authors: muenke m. Hum Mutat. 2000;16(2):99-108. doi: 10.1002/1098-1004(200008)16:2<99::AID-HUMU2>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10923031 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

323 results

Search Page