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Eis, Peggy S.
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1

Progressive multifocal leukoencephalopathy genetic risk var..:

Hatchwell, Eli ; Smith III, Edward B. ; Jalilzadeh, Shapour...
Frontiers in Neurology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

Germline Genetic Risk Variants for Progressive Multifocal L..:

Eis, Peggy S. ; Bruno, Christopher D. ; Richmond, Todd A....
Frontiers in Neurology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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3

Loss-of-Function NUBPL Mutation May Link Parkinson's Diseas..:

Eis, Peggy S. ; Huang, Neng ; Langston, J. William..
Frontiers in Neurology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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4

Genetic fine-mapping of the Iowan SNCA gene triplication in..:

Zafar, Faria ; Valappil, Ruksana Azhu ; Kim, Sam...
npj Parkinson's Disease.  4 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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5

The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinem..:

Richard, Anne Claire ; Rovelet‐Lecrux, Anne ; Delaby, Elsa...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  171 (2016)  3 - p. 377-382 , 2016
Link: https://doi.org/10.1002/..
 
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6

Comparative genomic hybridization solves a 14‐year‐old PARK..:

Schüle, Birgitt ; Hatchwell, Eli ; Eis, Peggy S..
Annals of Neurology.  78 (2015)  4 - p. 663-664 , 2015
Link: https://doi.org/10.1002/..
 
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7

Acquired Copy Number Alterations in Adult Acute Myeloid Leu..:

Walter, Matthew J. ; Payton, Jacqueline E. ; Ries, Rhonda E....
Proceedings of the National Academy of Sciences of the United States of America.  106 (2009)  31 - p. 12950-12955 , 2009
Link: https://www.jstor.org/st..
 
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8

Acquired copy number alterations in adult acute myeloid leu..:

Walter, Matthew J. ; Payton, Jacqueline E. ; Ries, Rhonda E....
Proceedings of the National Academy of Sciences.  106 (2009)  31 - p. 12950-12955 , 2009
Link: https://doi.org/10.1073/..
 
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9

wuHMM: a robust algorithm to detect DNA copy number variati..:

Cahan, Patrick ; Godfrey, Laura E. ; Eis, Peggy S....
Nucleic Acids Research.  36 (2008)  7 - p. e41 , 2008
Link: https://doi.org/10.1093/..
 
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10

A High-Resolution Map of Segmental DNA Copy Number Variatio..:

Graubert, Timothy A. ; Cahan, Patrick ; Edwin, Deepa...
PLoS Genetics.  3 (2007)  1 - p. e3 , 2007
Link: https://doi.org/10.1371/..
 
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11

Characterization of a recurrent 15q24 microdeletion syndrom:

Sharp, Andrew J. ; Selzer, Rebecca R. ; Veltman, Joris A....
Human Molecular Genetics.  16 (2007)  5 - p. 567-572 , 2007
Link: https://doi.org/10.1093/..
 
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12

Discovery of a previously unrecognized microdeletion syndro..:

Ballif, Blake C ; Hornor, Sara A ; Jenkins, Elizabeth...
Nature Genetics.  39 (2007)  9 - p. 1071-1073 , 2007
Link: https://doi.org/10.1038/..
 
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13

Discovery of previously unidentified genomic disorders from..:

Sharp, Andrew J ; Hansen, Sierra ; Selzer, Rebecca R...
Nature Genetics.  38 (2006)  9 - p. 1038-1042 , 2006
Link: https://doi.org/10.1038/..
 
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14

Accumulation of miR-155 and BIC RNA in Human B Cell Lymphom..:

Eis, Peggy S. ; Tam, Wayne ; Sun, Liping...
Proceedings of the National Academy of Sciences of the United States of America.  102 (2005)  10 - p. 3627-3632 , 2005
Link: https://www.jstor.org/st..
 
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15

Accumulation of miR-155 andBICRNA in human B cell lymphomas:

Eis, Peggy S. ; Tam, Wayne ; Sun, Liping...
Proceedings of the National Academy of Sciences.  102 (2005)  10 - p. 3627-3632 , 2005
Link: https://doi.org/10.1073/..
 
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