Konark Mukherjee

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Topics

Top Venues

Journal of medical genetics

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Paras A Patel, Leslie E W LaConte, Chen Liang, Thomas Cecere, Deepa Rajan, Sarika Srivastava, Konark Mukherjee
Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein. Journal of medical genetics 61 (8) (2024)
Paras A Patel, Leslie E W LaConte, Chen Liang, Thomas Cecere, Deepa Rajan, Sarika Srivastava, Konark Mukherjee
Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein. Journal of medical genetics 61 (8) (2024)
Paras A Patel, Leslie E W LaConte, Chen Liang, Thomas Cecere, Deepa Rajan, Sarika Srivastava, Konark Mukherjee
Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein. Journal of medical genetics (2024)
Paras A Patel, Leslie E W LaConte, Chen Liang, Thomas Cecere, Deepa Rajan, Sarika Srivastava, Konark Mukherjee
Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein. Journal of medical genetics 61 (8) (2024)
Paras A Patel, Leslie E W LaConte, Chen Liang, Thomas Cecere, Deepa Rajan, Sarika Srivastava, Konark Mukherjee
Genetic evidence for splicing-dependent structural and functional plasticity in CASK protein. Journal of medical genetics 61 (8) (2024)
Paras A Patel, Julia V Hegert, Ingrid Cristian, Alicia Kerr, Leslie E W LaConte, Michael A Fox, Sarika Srivastava, Konark Mukherjee
Complete loss of the X-linked gene CASK causes severe cerebellar degeneration. Journal of medical genetics 59 (11) (2022)
Konark Mukherjee, Paras A Patel, Deepa S Rajan, Leslie E W LaConte, Sarika Srivastava
Survival of a male patient harboring CASK Arg27Ter mutation to adolescence. Molecular genetics & genomic medicine 8 (10) (2020)
Carleigh Studtmann, Leslie E W LaConte, Konark Mukherjee
Comments on: A de novo in-frame deletion of CASK gene causes early onset infantile spasms and supratentorial cerebral malformation in a female patient. American journal of medical genetics. Part A 179 (12) (2019)
Leslie E W LaConte, Vrushali Chavan, Stephanie DeLuca, Karol Rubin, Jessica Malc, Susan Berry, C Gail Summers, Konark Mukherjee
An N-terminal heterozygous missense CASK mutation is associated with microcephaly and bilateral retinal dystrophy plus optic nerve atrophy. American journal of medical genetics. Part A 179 (1) (2018)