| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2015 | Zhao Y, Feng Y, Zhang YM, Ding XX, Song YZ, Zhang AM, Liu L, Zhang H, Ding JH, Xia XS. Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy. International Journal of Molecular Medicine. PMID 26458567 DOI: 10.3892/ijmm.2015.2361 | 0.371 | |||
| 2015 | Zhao Y, Feng Y, Zhang YM, Ding XX, Song YZ, Zhang AM, Liu L, Zhang H, Ding JH, Xia XS. Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy. Biomed Research International. 2015: 561819. PMID 26199943 DOI: 10.1155/2015/561819 | 0.342 | |||
| 2003 | Zhang LF, Ding JH, Yang BZ, He GC, Roe C. Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95. Genomics. 82: 660-8. PMID 14611808 DOI: 10.1016/S0888-7543(03)00211-8 | 0.397 | |||
| 2001 | Yang BZ, Mallory JM, Roe DS, Brivet M, Strobel GD, Jones KM, Ding JH, Roe CR. Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family. Molecular Genetics and Metabolism. 73: 64-70. PMID 11350184 DOI: 10.1006/Mgme.2001.3162 | 0.466 | |||
| 2000 | Yang B, Ding J, Zhou C, Dimachkie MM, Sweetman L, Dasouki MJ, Wilkinson J, Roe CR. Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency. Molecular Genetics and Metabolism. 69: 259-262. PMID 10767181 DOI: 10.1006/Mgme.2000.2978 | 0.431 | |||
| 1999 | He G, Yang B, Roe DS, Teramoto R, Aleck K, Grebe TA, Roe CR, Ding J. Identification Of Two Novel Mutations In The Hypoglycemic Phenotype Of Very Long Chain Acyl-Coa Dehydrogenase Deficiency Biochemical and Biophysical Research Communications. 264: 483-487. PMID 10529389 DOI: 10.1006/Bbrc.1999.1411 | 0.487 | |||
| 1998 | Yang B, Ding J, Dewese T, Roe D, He G, Wilkinson J, Day DW, Rabier D, Brivet M, Roe C. Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency Molecular Genetics and Metabolism. 64: 229-236. PMID 9758712 DOI: 10.1006/Mgme.1998.2711 | 0.469 | |||
| 1998 | Yang B, Ding J, Roe D, Dewese T, Day DW, Roe CR. A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency Molecular Genetics and Metabolism. 63: 110-115. PMID 9562964 DOI: 10.1006/Mgme.1997.2656 | 0.474 | |||
| 1996 | Yang B, Heng HHQ, Ding J, Roe CR. The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23 Genomics. 37: 141-143. PMID 8921383 DOI: 10.1006/Geno.1996.0533 | 0.338 | |||
| 1996 | Ding J, Yang B, Nada MA, Roe CR. Improved Detection of the G1528C Mutation in LCHAD Deficiency Biochemical and Molecular Medicine. 58: 46-51. PMID 8809345 DOI: 10.1006/Bmme.1996.0031 | 0.461 | |||
| 1996 | Nada MA, Vianey-Saban C, Roe CR, Ding J, Mathieu M, Wappner RS, Bialer MG, Mcglynn JA, Mandon G. Prenatal diagnosis of mitochondrial fatty acid oxidation defects. Prenatal Diagnosis. 16: 117-124. PMID 8650121 DOI: 10.1002/(Sici)1097-0223(199602)16:2<117::Aid-Pd820>3.0.Co;2-Z | 0.376 | |||
| Low-probability matches (unlikely to be authored by this person) | |||||
| 2006 | Chen S, Ding JH, Bekeredjian R, Yang BZ, Shohet RV, Johnston SA, Hohmeier HE, Newgard CB, Grayburn PA. Efficient gene delivery to pancreatic islets with ultrasonic microbubble destruction technology. Proceedings of the National Academy of Sciences of the United States of America. 103: 8469-74. PMID 16709667 DOI: 10.1073/Pnas.0602921103 | 0.166 | |||
| Hide low-probability matches. | |||||