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

Papers共 48 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
Expanding the Phenotypic Spectrum of CSNK2A1-associated Okur-Chung Neurodevelopmental Syndrome
Swetha Ramadesikan, Iftekhar A. Showpnil,Mohammad Marhabaie, Allison Daley, Elizabeth A. Varga, Umamaheswaran Gurusamy,Matthew T. Pastore, Emily R. Sites, Murugu Manickam,Dennis W. Bartholomew,Jesse M. Hunter,Peter White,Richard K. Wilson, Rolf W. Stottmann,Daniel C. Koboldt
Human Genetics and Genomics Advancespp.100379, (2024)
Cited0Views0WOSBibtex
0
0
Long-read Genome Sequencing Resolves Complex Genomic Rearrangements in Rare Genetic Syndromes
Iftekhar A. Showpnil, Maria E. Hernandez Gonzalez,Swetha Ramadesikan,Mohammad Marhabaie, Allison Daley, Leeran Dublin-Ryan,Matthew T. Pastore, Umamaheswaran Gurusamy,Jesse M. Hunter, Brandon S. Stone,Dennis W. Bartholomew,Kandamurugu Manickam,Anthony R. Miller,Richard K. Wilson, Rolf W. Stottmann,Daniel C. Koboldt
NPJ GENOMIC MEDICINEno. 1 (2024)
Cited0Views0WOSNATUREBibtex
0
0
Load More
Author Statistics

#Papers: 48

#Citation: 1590

H-Index: 19

G-Index: 35

Sociability: 7

Diversity: 3

Activity: 8

  • 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