Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.
Research Interests

Papers共 6 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Burden of Rare Genetic Disorders in India: Twenty-Two Years’ Experience of a Tertiary Centre
Jayesh Sheth,Aadhira Nair,Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Inusha Panigrahi,Ashish Bavdekar,Sheela Nampoothiri,Chaitanya Datar, Ajit Gandhi,Mamta Muranjan,Anupriya Kaur, Manisha Desai,Mehul Mistri, Chitra Patel,Premal Naik,Maulin Shah,Koumudi Godbole,Seema Kapoor,Neerja Gupta,Sunita Bijarnia-Mahay, Sandeep Kadam,Dhaval Solanki, Soham Desai, Anand Iyer,Ketan Patel,Harsh Patel,Raju C. Shah, Shalmi Mehta, Ruchi Shah,Riddhi Bhavsar,Jhanvi Shah, Mili Pandya, Bhagyadhan Patel,Sudhir Shah,Heli Shah,Shalin Shah,Shruti Bajaj,Siddharth Shah, Nilam Thaker,Umesh Kalane,Mahesh Kamate, Vykunta Raju KN,Naresh Tayade, Sujatha Jagadeesan,Deepika Jain,Mitesh Chandarana, Jitendra Singh,Sanjiv Mehta,Beena Suresh,Harsh Sheth
ORPHANET JOURNAL OF RARE DISEASESno. 1 (2024)
Cited0Views0WOSBibtex
0
0
Author Statistics

#Papers: 6

#Citation: 12

H-Index: 2

G-Index: 3

Sociability: 4

Diversity: 1

Activity: 1

  • 合作者
  • 学生
  • 导师
No result temporarily, you can search similar Scholar with the same research interest
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn