Christian Vaisse, M.D., Ph.D. - Related publications

Diabetes Center University of California, San Francisco, San Francisco, CA 
Genetics of Obesity
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12 most relevant papers in past 60 days:
Year Citation  Score
2022 Jiang Z, Cai X, Kong J, Zhang R, Ding Y. Maternally transmitted diabetes mellitus may be associated with mitochondrial ND5 T12338C and tRNA T5587C variants. Irish Journal of Medical Science. PMID 34993838 DOI: 10.1007/s11845-021-02911-w   
2022 Kwon YJ, Park DH, Choi JE, Lee D, Hong KW, Lee JW. Identification of the interactions between specific genetic polymorphisms and nutrient intake associated with general and abdominal obesity in middle-aged adults. Clinical Nutrition (Edinburgh, Scotland). 41: 543-551. PMID 35030529 DOI: 10.1016/j.clnu.2021.12.040   
2022 Liu YD, Huang SS, Li M, Lek M, Song DY, Tan DD, Chen XY, Zhang H, Liu JY, Chang XZ, Xiong H. A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11. Clinical Genetics. PMID 34988992 DOI: 10.1111/cge.14108   
2022 Abdelrahman HA, Akawi N, Al-Shamsi AM, Ali A, Al-Jasmi F, John A, Hertecant J, Al-Gazali L, Ali BR. Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive. Clinical Genetics. PMID 34988996 DOI: 10.1111/cge.14107   
2022 Zhang Y, Lin C, Chen R, Luo L, Huang J, Liu H, Chen W, Xu J, Yu H, Ding Y. Association analysis of SOCS3, JAK2 and STAT3 gene polymorphisms and genetic susceptibility to type 2 diabetes mellitus in Chinese population. Diabetology & Metabolic Syndrome. 14: 4. PMID 34991691 DOI: 10.1186/s13098-021-00774-w   
2022 Chapla A, Johnson J, Korula S, Mohan N, Ahmed A, Varghese D, Rangasamy P, Ravichandran L, Jebasingh F, Agrawal KK, Somasundaram N, Hesarghatta Shyamasunder A, Mathai S, Simon A, Jha S, et al. WFS1 gene associated diabetes phenotypes and identification of a founder mutation in Southern India. The Journal of Clinical Endocrinology and Metabolism. PMID 35018440 DOI: 10.1210/clinem/dgac002   
2022 Dong J, Fu J, Yan Z, Li L, Qiu Y, Zeng Y, Liu R, Chen B, Shi R, Diao F, Wang L, Shi Q, Sang Q. Novel biallelic mutations in PADI6 in patients with early embryonic arrest. Journal of Human Genetics. PMID 34987164 DOI: 10.1038/s10038-021-00998-8   
2022 Zhou C, Wang J, Zhang Q, Yang Q, Yi S, Shen Y, Luo J, Qin Z. Clinical and genetic analysis of combined oxidative phosphorylation defificiency-10 caused by MTO1 mutation. Clinica Chimica Acta; International Journal of Clinical Chemistry. PMID 34990597 DOI: 10.1016/j.cca.2021.12.025   
2022 Sun Y, Lin W, Dong W, Xu J. Origin and evolutionary analysis of the SARS-CoV-2 Omicron variant. Journal of Biosafety and Biosecurity. 4: 33-37. PMID 35005525 DOI: 10.1016/j.jobb.2021.12.001   
2022 Liu CY, Lin JL, Feng SY, Che CH, Huang HP, Zou ZY. Novel Variants in the Gene Associated With Chinese Sporadic Amyotrophic Lateral Sclerosis With Slow Progression. Journal of Clinical Neurology (Seoul, Korea). 18: 41-47. PMID 35021275 DOI: 10.3988/jcn.2022.18.1.41   
2022 Wang Z, Zhou L, Lan Y, Li X, Wang J, Dong J, Guo W, Jing D, Liu Q, Zhang S, Liu Z, Shi W, Yang W, Yang T, Sun F, et al. An aspartic protease 47 causes quantitative recessive resistance to rice black-streaked dwarf virus disease and southern rice black-streaked dwarf virus disease. The New Phytologist. PMID 35015901 DOI: 10.1111/nph.17961   
2022 Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, ... , et al. The genetic architecture of pediatric cardiomyopathy. American Journal of Human Genetics. PMID 35026164 DOI: 10.1016/j.ajhg.2021.12.006