Gong M - Search Results

1

Childhood hypertension in autosomal-dominant hypertension with brachydactyly.

Toka O, Maass PG, Aydin A, Toka H, Hübner N, Rüschendorf F, Gong M, Luft FC, Bähring S. Toka O, et al. Among authors: gong m. Hypertension. 2010 Nov;56(5):988-94. doi: 10.1161/HYPERTENSIONAHA.110.156620. Epub 2010 Sep 13. Hypertension. 2010. PMID: 20837885

2

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p.

Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bähring S, Luft FC, Nürnberg P, Reis A, Rohde K, Ganten D, Hui R, Hübner N. Gong M, et al. Hum Mol Genet. 2003 Jun 1;12(11):1273-7. doi: 10.1093/hmg/ddg135. Hum Mol Genet. 2003. PMID: 12761042

3

Molecular genetics of human hypertension.

Gong M, Hubner N. Gong M, et al. Clin Sci (Lond). 2006 Mar;110(3):315-26. doi: 10.1042/CS20050208. Clin Sci (Lond). 2006. PMID: 16464173 Review.

4

Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.

Lee-Kirsch MA, Gong M, Schulz H, Rüschendorf F, Stein A, Pfeiffer C, Ballarini A, Gahr M, Hubner N, Linné M. Lee-Kirsch MA, et al. Among authors: gong m. Am J Hum Genet. 2006 Oct;79(4):731-7. doi: 10.1086/507848. Epub 2006 Aug 17. Am J Hum Genet. 2006. PMID: 16960810 Free PMC article.

5

Quantitative genetic basis of arterial phenotypes in the Brown Norway rat.

Kota L, Osborne-Pellegrin M, Schulz H, Behmoaras J, Coutard M, Gong M, Hübner N. Kota L, et al. Among authors: gong m. Physiol Genomics. 2007 Jun 19;30(1):17-25. doi: 10.1152/physiolgenomics.00209.2006. Epub 2007 Mar 13. Physiol Genomics. 2007. PMID: 17356016

6

Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA.

Bähring S, Kann M, Neuenfeld Y, Gong M, Chitayat D, Toka HR, Toka O, Plessis G, Maass P, Rauch A, Aydin A, Luft FC. Bähring S, et al. Among authors: gong m. Hypertension. 2008 Feb;51(2):426-31. doi: 10.1161/HYPERTENSIONAHA.107.101774. Epub 2007 Dec 17. Hypertension. 2008. PMID: 18086950

7

Two novel GATA6 mutations cause childhood-onset diabetes mellitus, pancreas malformation and congenital heart disease.

Gong M, Simaite D, Kühnen P, Heldmann M, Spagnoli F, Blankenstein O, Hübner N, Hussain K, Raile K. Gong M, et al. Horm Res Paediatr. 2013;79(4):250-6. doi: 10.1159/000348844. Epub 2013 Apr 26. Horm Res Paediatr. 2013. PMID: 23635550

8

Recessive mutations in PCBD1 cause a new type of early-onset diabetes.

Simaite D, Kofent J, Gong M, Rüschendorf F, Jia S, Arn P, Bentler K, Ellaway C, Kühnen P, Hoffmann GF, Blau N, Spagnoli FM, Hübner N, Raile K. Simaite D, et al. Among authors: gong m. Diabetes. 2014 Oct;63(10):3557-64. doi: 10.2337/db13-1784. Epub 2014 May 21. Diabetes. 2014. PMID: 24848070 Free article.

9

PDE3A mutations cause autosomal dominant hypertension with brachydactyly.

Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S. Maass PG, et al. Among authors: gong m. Nat Genet. 2015 Jun;47(6):647-53. doi: 10.1038/ng.3302. Epub 2015 May 11. Nat Genet. 2015. PMID: 25961942 Free article.

10

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.

Su X, Feng Y, Rahman SA, Wu S, Li G, Rüschendorf F, Zhao L, Cui H, Liang J, Fang L, Hu H, Froehler S, Yu Y, Patone G, Hummel O, Chen Q, Raile K, Luft FC, Bähring S, Hussain K, Chen W, Zhang J, Gong M. Su X, et al. Among authors: gong m. J Genet Genomics. 2020 Oct 20;47(10):618-626. doi: 10.1016/j.jgg.2020.07.008. Epub 2020 Oct 28. J Genet Genomics. 2020. PMID: 33358777

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