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Sambuughin, Nyamkhishig
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1

Genome-Wide Analysis of Exertional Rhabdomyolysis in Sickle..:

Ren, Mingqiang ; Sambuughin, Nyamkhishig ; Mungunshukh, Ognoon...
Genes.  15 (2024)  4 - p. 408 , 2024
Link: https://doi.org/10.3390/..
 
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2

Optimization of Omega-3 Index Levels in Athletes at the US ..:

Rittenhouse, Melissa ; Sambuughin, Nyamkhishig ; Deuster, Patricia
Nutrients.  14 (2022)  14 - p. 2966 , 2022
Link: https://doi.org/10.3390/..
 
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3

Updated variant curation expert panel criteria and pathogen..:

Johnston, Jennifer J ; Dirksen, Robert T ; Girard, Thierry...
Human Molecular Genetics.  31 (2022)  23 - p. 4087-4093 , 2022
Link: https://doi.org/10.1093/..
 
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4

eP364: Lessons from pathogenicity classifications for 251 R..:

Johnston, Jennifer ; Dirksen, Robert ; Girard, Thierry...
Genetics in Medicine.  24 (2022)  3 - p. S229-S230 , 2022
Link: https://doi.org/10.1016/..
 
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5

Variant curation expert panel recommendations for RYR1 path..:

Johnston, Jennifer J. ; Dirksen, Robert T. ; Girard, Thierry...
Genetics in Medicine.  23 (2021)  7 - p. 1288-1295 , 2021
Link: https://doi.org/10.1038/..
 
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6

Multifactorial Origin of Exertional Rhabdomyolysis, Recurre..:

Sambuughin, Nyamkhishig ; Ren, Mingqiang ; Capacchione, John F....
Case Reports in Genetics.  2018 (2018)  - p. 1-6 , 2018
Link: https://doi.org/10.1155/..
 
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7

Response to Finsterer and Zarrouk-Mahjoub:

Sambuughin, Nyamkhishig ; Smith, Jonathan ; O'Connor, Francis.
Molecular Genetics and Metabolism Reports.  17 (2018)  - p. 2 , 2018
Link: https://doi.org/10.1016/..
 
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8

Pathogenic and rare deleterious variants in multiple genes ..:

Sambuughin, Nyamkhishig ; Mungunsukh, Ognoon ; Ren, Mingqiang...
Molecular Genetics and Metabolism Reports.  16 (2018)  - p. 76-81 , 2018
Link: https://doi.org/10.1016/..
 
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9

Adult-onset autosomal dominant spastic paraplegia linked to..:

Sambuughin, Nyamkhishig ; Goldfarb, Lev G. ; Sivtseva, Tatiana M....
BMC Neurology.  15 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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10

A new disease allele for the p.C30071R mutation in titin ca..:

Pfeffer, Gerald ; Sambuughin, Nyamkhishig ; Olivé, Montse...
Neuromuscular Disorders.  24 (2014)  3 - p. 241-244 , 2014
Link: https://doi.org/10.1016/..
 
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11

Exome analysis identifies Brody myopathy in a family diagno..:

Sambuughin, Nyamkhishig ; Zvaritch, Elena ; Kraeva, Natasha...
Molecular Genetics & Genomic Medicine.  2 (2014)  6 - p. 472-483 , 2014
Link: https://doi.org/10.1002/..
 
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12

Exome sequencing identifies titin mutations causing heredit..:

Toro, Camilo ; Olivé, Montse ; Dalakas, Marinos C...
BMC Neurology.  13 (2013)  1 - p. , 2013
Link: https://doi.org/10.1186/..
 
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13

Exome sequencing reveals SCO2 mutations in a family present..:

Sambuughin, Nyamkhishig ; Liu, Xinyue ; Bijarnia, Sunita...
Journal of Human Genetics.  58 (2013)  4 - p. 226-228 , 2013
Link: https://doi.org/10.1038/..
 
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14

Genetic variants in potassium channels are associated with ..:

ODGEREL, Zagaa ; LEE, Hee S. ; ERDENEBILEG, Narnygerel...
Journal of Diabetes.  4 (2012)  3 - p. 238-242 , 2012
Link: https://doi.org/10.1111/..
 
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15

Investigation of the Relationship Between Serum Creatine Ki..:

Landau, Mark E. ; Kenney, Kimbra ; Deuster, Patricia...
Military Medicine.  177 (2012)  11 - p. 1359-1365 , 2012
Link: https://doi.org/10.7205/..
 
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