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/vufind/Search/Results?lookfor=%22Russell%2C+Kathryn%22&type=Person&sort=year
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PubPharm (146)
1
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
enthalten in:
bioRxiv.org
| 2024
von
Lemire, G.
|
Sanchis-Juan, A.
|
Russell, K.
| +61
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2
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
enthalten in:
bioRxiv.org
| 2024
von
Jurgens, J.
|
Barry, B.
|
Chan, W.
| +37
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3
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
enthalten in:
American journal of human genetics
| 2024
von
Lemire, G.
|
Sanchis-Juan, A.
|
Russell, K.
| +61
UpdateOf: medRxiv. 2023 Oct 05;:. - PMID 37873196
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4
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
enthalten in:
medRxiv : the preprint server for health sciences
| 2024
von
Jurgens, J.
|
Barry, B.
|
Chan, W.
| +38
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5
Time independent factors that predict relapse in adults with acute myeloid leukemia
enthalten in:
Blood cancer journal
| 2024
von
Lim, J.
|
Othus, M.
|
Shaw, C.
| +7
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6
When the implementation of water safety plans fail : rethinking the approach to water safety planning following a serious waterborne outbreak and implications for subsequent water sector reforms
enthalten in:
Journal of water and health
| 2023
von
Graham, J.
|
Russell, K.
|
Gilpin, B.
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7
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Lemire, G.
|
Sanchis-Juan, A.
|
Russell, K.
| +61
UpdateIn: Am J Hum Genet. 2024 Mar 27;:. - PMID 38565148
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8
Sleep health behaviors in pediatric patients with newly diagnosed cancer
enthalten in:
Journal of psychosomatic research
| 2023
von
Tucker, P.
|
Loew, M.
|
Russell, K.
| +5
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9
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
enthalten in:
bioRxiv.org
| 2023
von
Wojcik, M.
|
Lemire, G.
|
Zaki, M.
| +72
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10
Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Wojcik, M.
|
Lemire, G.
|
Zaki, M.
| +72
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