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个人简介
My laboratory is interested in identifying and understanding the function of genes which cause a variety of human disorders. Our research efforts have focused on the molecular genetics of monogenic disorders, as well as polygenic and multifactorial disorders. Our research efforts have resulted in the mapping of many different disease loci. In addition, we have used positional cloning methods to identify genes involved in a number of different diseases including hereditary blindness and deafness. Efforts are currently underway to use positional cloning strategies to identify additional disease-causing genes. Complex genetic disorders currently under investigation in the laboratory include hypertension, obesity, congenital heart disease and autism. In addition, we have worked on developing and improving techniques for disease mapping, positional cloning, and mutation detection. We have also had an active role in the human genome project and the rat genome project.
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Shruti V. Patil, Balasankara Reddy Kaipa, Sujata Ranshing, Yogapriya Sundaresan,J. Cameron Millar,Bhavani Nagarajan,Charles Kiehlbauch,Qihong Zhang,Ankur Jain,Charles C. Searby,Todd E. Scheetz, Abbot F. Clark,
Research squareno. 1 (2024): 6958-6958
Functionno. 1 (2023): zqad070-zqad070
Physiologyno. S1 (2023)
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Sara K Mayer,Jacintha Thomas,Megan Helms, Aishwarya Kothapalli Kothapalli,Ioana Cherascu,Elliot Stalter,Kai Wang,Poppy Datta,Charles Searby,Seongjin Seo,Ying Hsu,Sajag Bhattarai,
Sunny C Huang,Thomas K Pak, Cameron P Graber,Charles C Searby, Guanghao Liu, Jennifer Marcy, Alexandra K Yaszemski,Kurt Bedell, Emily Bui,Stanley Perlman,Qihong Zhang,Kai Wang,
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