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Matsushita, Mark
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1

Novel TREM2 splicing isoform that lacks the V-set immunoglo..:

Kiianitsa, Kostantin ; Kurtz, Irina ; Beeman, Neal...
Journal of Leukocyte Biology.  110 (2021)  5 - p. 829-837 , 2021
Link: https://doi.org/10.1002/..
 
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2

Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacer..:

Korvatska, Olena ; Kiianitsa, Kostantin ; Ratushny, Alexander...
Frontiers in Immunology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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3

De novo microdeletion of BCL11A is associated with severe s..:

Peter, Beate ; Matsushita, Mark ; Oda, Kaori.
American Journal of Medical Genetics Part A.  164 (2014)  8 - p. 2091-2096 , 2014
Link: https://doi.org/10.1002/..
 
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4

A Novel Spinocerebellar Ataxia With Hematologic Cytopenias:..:

Chen, Dong-Hui ; Below, Piper ; Sul, Youngmee...
Neurology.  82 (2014)  10_supplement - p. , 2014
Link: https://doi.org/10.1212/..
 
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5

Evidence for involvement of GNB1L in autism:

Chen, Ying‐Zhang ; Matsushita, Mark ; Girirajan, Santhosh...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  159B (2011)  1 - p. 61-71 , 2011
Link: https://doi.org/10.1002/..
 
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6

Genome Scan for Spelling Deficits: Effects of Verbal IQ on ..:

Rubenstein, Kevin ; Matsushita, Mark ; Berninger, Virginia W...
Behavior Genetics.  41 (2010)  1 - p. 31-42 , 2010
Link: https://doi.org/10.1007/..
 
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7

A novel X‐linked four‐repeat tauopathy with Parkinsonism an..:

Poorkaj, Parvoneh ; Raskind, Wendy H. ; Leverenz, James B....
Movement Disorders.  25 (2010)  10 - p. 1409-1417 , 2010
Link: https://doi.org/10.1002/..
 
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8

A novel mutation in FHL1 in a family with X-linked scapulop..:

Chen, Dong-Hui ; Raskind, Wendy H. ; Parson, William W....
Journal of the Neurological Sciences.  296 (2010)  1-2 - p. 22-29 , 2010
Link: https://doi.org/10.1016/..
 
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9

Replication of CNTNAP2 association with nonword repetition ..:

Peter, Beate ; Raskind, Wendy H. ; Matsushita, Mark...
Journal of Neurodevelopmental Disorders.  3 (2010)  1 - p. 39-49 , 2010
Link: https://doi.org/10.1007/..
 
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10

Familial dyskinesia and facial myokymia (FDFM): Follow‐up o..:

Raskind, Wendy H. ; Matsushita, Mark ; Peter, Beate...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  150B (2008)  4 - p. 570-574 , 2008
Link: https://doi.org/10.1002/..
 
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11

Sensorineural deafness, distinctive facial features, and ab..:

Gad, Alona ; Laurino, Mercy ; Maravilla, Kenneth R...
American Journal of Medical Genetics Part A.  146A (2008)  14 - p. 1880-1885 , 2008
Link: https://doi.org/10.1002/..
 
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12

Genomewide scan for real‐word reading subphenotypes of dysl..:

Igo Jr, Robert P. ; Chapman, Nicola H. ; Berninger, Virginia W....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  141B (2005)  1 - p. 15-27 , 2005
Link: https://doi.org/10.1002/..
 
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13

Linkage analyses of four regions previously implicated in d..:

Chapman, Nicola H. ; Igo, Robert P. ; Thomson, Jennifer B....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  131B (2004)  1 - p. 67-75 , 2004
Link: https://doi.org/10.1002/..
 
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14

Autosomal dominant sensory/motor neuropathy with Ataxia (SM..:

Brkanac, Zoran ; Fernandez, Magali ; Matsushita, Mark...
American Journal of Medical Genetics.  114 (2002)  4 - p. 450-457 , 2002
Link: https://doi.org/10.1002/..
 
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15

Familial dyskinesia and facial myokymia (FDFM): A novel mov..:

Fernandez, Magali ; Raskind, Wendy ; Wolff, John...
Annals of Neurology.  49 (2001)  4 - p. 486-492 , 2001
Link: https://doi.org/10.1002/..
 
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