Mohr J - Search Results

1

Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits.

Lohoff FW, Lautenschlager M, Mohr J, Ferraro TN, Sander T, Gallinat J. Lohoff FW, et al. Among authors: mohr j. Neurosci Lett. 2008 Mar 21;434(1):41-5. doi: 10.1016/j.neulet.2008.01.024. Epub 2008 Jan 16. Neurosci Lett. 2008. PMID: 18249496

2

The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children.

Rowe DC, Stever C, Gard JM, Cleveland HH, Sanders ML, Abramowitz A, Kozol ST, Mohr JH, Sherman SL, Waldman ID. Rowe DC, et al. Among authors: mohr jh. Behav Genet. 1998 May;28(3):215-25. doi: 10.1023/a:1021427314941. Behav Genet. 1998. PMID: 9670597

3

Dopamine DRD4 receptor polymorphism and attention deficit hyperactivity disorder.

Rowe DC, Stever C, Giedinghagen LN, Gard JM, Cleveland HH, Terris ST, Mohr JH, Sherman S, Abramowitz A, Waldman ID. Rowe DC, et al. Among authors: mohr jh. Mol Psychiatry. 1998 Sep;3(5):419-26. doi: 10.1038/sj.mp.4000432. Mol Psychiatry. 1998. PMID: 9774775

4

Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity.

Waldman ID, Rowe DC, Abramowitz A, Kozel ST, Mohr JH, Sherman SL, Cleveland HH, Sanders ML, Gard JM, Stever C. Waldman ID, et al. Among authors: mohr jh. Am J Hum Genet. 1998 Dec;63(6):1767-76. doi: 10.1086/302132. Am J Hum Genet. 1998. PMID: 9837830 Free PMC article.

5

The DRD2 TaqI polymorphism and symptoms of attention deficit hyperactivity disorder.

Rowe DC, Van den Oord EJ, Stever C, Giedinghagen LN, Gard JM, Cleveland HH, Gilson M, Terris ST, Mohr JH, Sherman S, Abramowitz A, Waldman ID. Rowe DC, et al. Among authors: mohr jh. Mol Psychiatry. 1999 Nov;4(6):580-6. doi: 10.1038/sj.mp.4000567. Mol Psychiatry. 1999. PMID: 10578241

6

Executive function in children with Tourette syndrome and/or attention deficit hyperactivity disorder.

Harris EL, Schuerholz LJ, Singer HS, Reader MJ, Brown JE, Cox C, Mohr J, Chase GA, Denckla MB. Harris EL, et al. Among authors: mohr j. J Int Neuropsychol Soc. 1995 Nov;1(6):511-6. doi: 10.1017/s1355617700000631. J Int Neuropsychol Soc. 1995. PMID: 9375237

7

An analysis of two discrepancy-based models and a processing-deficit approach in identifying learning disabilities.

Schuerholz LJ, Harris EL, Baumgardner TL, Reiss AL, Freund LS, Church RP, Mohr J, Denckla MB. Schuerholz LJ, et al. Among authors: mohr j. J Learn Disabil. 1995 Jan;28(1):18-29. doi: 10.1177/002221949502800104. J Learn Disabil. 1995. PMID: 7844483

8

Novel variants in the SOX11 gene: clinical description of seven new patients.

Schincariol-Manhe B, Campagnolo É, Spineli-Silva S, de Leeuw N, Correia-Costa GR, Pessoa A, de Souza CFM, Stevens C, Javaher P, Scallet HF, Mohr J, Biskup S, Herkert JC, Pfundt R, Mehta L, Rekab A, Elloumi HZ, Sanyoura M, Maciel-Guerra AT, Gil-da-Silva-Lopes VL, Dos Santos AM, Vieira TP. Schincariol-Manhe B, et al. Among authors: mohr j. Eur J Hum Genet. 2024 Sep 27. doi: 10.1038/s41431-024-01695-8. Online ahead of print. Eur J Hum Genet. 2024. PMID: 39333428

9

Severe mixed hand and generalized eczema treated with the JAK inhibitor upadacitinib.

Cramer N, Mohr J, Schön MP, Mössner R. Cramer N, et al. Among authors: mohr j. J Dtsch Dermatol Ges. 2024 Sep 27. doi: 10.1111/ddg.15532. Online ahead of print. J Dtsch Dermatol Ges. 2024. PMID: 39331029 No abstract available.

10

Ratiometric near infrared fluorescence imaging of dopamine with 1D and 2D nanomaterials.

Hill BF, Mohr JM, Sandvoss IK, Gretz J, Galonska P, Schnitzler L, Erpenbeck L, Kruss S. Hill BF, et al. Among authors: mohr jm. Nanoscale. 2024 Oct 10;16(39):18534-18544. doi: 10.1039/d4nr02358g. Nanoscale. 2024. PMID: 39279544

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