Harvard Catalyst Profiles

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Ganeshwaran H. Mochida, M.D.

Co-Author

This page shows the publications co-authored by Ganeshwaran Mochida and Christopher Walsh.
Connection Strength

4.703
  1. CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nat Genet. 2012 Nov; 44(11):1260-4.
    View in: PubMed
    Score: 0.538
  2. A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Am J Hum Genet. 2010 Dec 10; 87(6):882-9.
    View in: PubMed
    Score: 0.473
  3. A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. Am J Hum Genet. 2009 Dec; 85(6):897-902.
    View in: PubMed
    Score: 0.442
  4. Broader geographical spectrum of Cohen syndrome due to COH1 mutations. J Med Genet. 2004 Jun; 41(6):e87.
    View in: PubMed
    Score: 0.302
  5. Genetic basis of developmental malformations of the cerebral cortex. Arch Neurol. 2004 May; 61(5):637-40.
    View in: PubMed
    Score: 0.300
  6. Molecular genetics of human microcephaly. Curr Opin Neurol. 2001 Apr; 14(2):151-6.
    View in: PubMed
    Score: 0.242
  7. Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genet Med. 2020 06; 22(6):1040-1050.
    View in: PubMed
    Score: 0.225
  8. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Rep. 2018 07 24; 24(4):973-986.e8.
    View in: PubMed
    Score: 0.201
  9. Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. Genome Res. 2017 08; 27(8):1323-1335.
    View in: PubMed
    Score: 0.186
  10. Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate. Neuron. 2016 Nov 23; 92(4):813-828.
    View in: PubMed
    Score: 0.178
  11. Loss of PCLO function underlies pontocerebellar hypoplasia type III. Neurology. 2015 Apr 28; 84(17):1745-50.
    View in: PubMed
    Score: 0.160
  12. Katanin p80 regulates human cortical development by limiting centriole and cilia number. Neuron. 2014 Dec 17; 84(6):1240-57.
    View in: PubMed
    Score: 0.157
  13. METTL23, a transcriptional partner of GABPA, is essential for human cognition. Hum Mol Genet. 2014 Jul 01; 23(13):3456-66.
    View in: PubMed
    Score: 0.148
  14. Using whole-exome sequencing to identify inherited causes of autism. Neuron. 2013 Jan 23; 77(2):259-73.
    View in: PubMed
    Score: 0.137
  15. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]. Am J Hum Genet. 2011 May 13; 88(5):536-47.
    View in: PubMed
    Score: 0.122
  16. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat Genet. 2010 Nov; 42(11):1015-20.
    View in: PubMed
    Score: 0.117
  17. Developmental and degenerative features in a complicated spastic paraplegia. Ann Neurol. 2010 Apr; 67(4):516-25.
    View in: PubMed
    Score: 0.113
  18. An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation. . 2006 Jul 15; 140(14):1504-10.
    View in: PubMed
    Score: 0.087
  19. ASPM mutations identified in patients with primary microcephaly and seizures. J Med Genet. 2005 Sep; 42(9):725-9.
    View in: PubMed
    Score: 0.082
  20. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology. 2003 May 27; 60(10):1664-7.
    View in: PubMed
    Score: 0.070
  21. Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. Eur J Hum Genet. 2021 Aug 20.
    View in: PubMed
    Score: 0.062
  22. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum Mol Genet. 2001 Aug 15; 10(17):1775-83.
    View in: PubMed
    Score: 0.062
  23. PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. . 2018 12; 177(8):736-745.
    View in: PubMed
    Score: 0.051
  24. Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures. . 2016 Feb; 170A(2):435-440.
    View in: PubMed
    Score: 0.041
  25. Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. Am J Hum Genet. 2014 Apr 03; 94(4):547-58.
    View in: PubMed
    Score: 0.037
  26. Posterior fossa in primary microcephaly: relationships between forebrain and mid-hindbrain size in 110 patients. Neuropediatrics. 2014 Apr; 45(2):93-101.
    View in: PubMed
    Score: 0.036
  27. Delineation of the clinical, molecular and cellular aspects of novel JAM3 mutations underlying the autosomal recessive hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Hum Mutat. 2013 Mar; 34(3):498-505.
    View in: PubMed
    Score: 0.035
  28. A novel form of lethal microcephaly with simplified gyral pattern and brain stem hypoplasia. . 2007 Dec 01; 143A(23):2761-7.
    View in: PubMed
    Score: 0.024
  29. The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle protein. Hum Mol Genet. 2005 Aug 01; 14(15):2155-65.
    View in: PubMed
    Score: 0.020
  30. Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion. PLoS Biol. 2004 May; 2(5):E126.
    View in: PubMed
    Score: 0.019
  31. Protein-truncating mutations in ASPM cause variable reduction in brain size. Am J Hum Genet. 2003 Nov; 73(5):1170-7.
    View in: PubMed
    Score: 0.018
  32. ASPM is a major determinant of cerebral cortical size. Nat Genet. 2002 Oct; 32(2):316-20.
    View in: PubMed
    Score: 0.017
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.