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Ek, Marlene
14  Ergebnisse:
Personensuche X
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1

Uncommon Variants in FLG2 and NOD2 Are Associated with Atop..:

Wang, Sailan ; Elmgren, Julia K. ; Eisfeldt, Jesper...
JID Innovations.  4 (2024)  4 - p. 100284 , 2024
Link: https://doi.org/10.1016/..
 
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2

A combination of long and short read genomics reveals frequ..:

Schuy, Jakob ; Sæther, Kristine Bilgrav ; Lisfeld, Jasmin...
Genetics in Medicine Open.  , 2024
Link: https://doi.org/10.1016/..
 
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3

Long-read sequencing and optical mapping generates near T2T..:

ten Berk de Boer, Esmee ; Ameur, Adam ; Bunikis, Ignas...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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4

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Pathology.  55 (2023)  - p. S19-S20 , 2023
Link: https://doi.org/10.1016/..
 
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5

Genome sequencing with comprehensive variant calling identi..:

Ek, Marlene ; Nilsson, Daniel ; Engvall, Martin...
Frontiers in Neurology.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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6

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Genetics in Medicine.  24 (2022)  11 - p. 2296-2307 , 2022
Link: https://doi.org/10.1016/..
 
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7

Genome sequencing with comprehensive variant calling identi..:

Ek, Marlene ; Nilsson, Daniel ; Engvall, Martin...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234573/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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8

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Genetics in Medicine, 1098-3600, 2022, 24:11, s. 2296-2307.  , 2022
Link: http://urn.kb.se/resolve..
 
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9

Table_4_Genome sequencing with comprehensive variant callin..:

Marlene Ek ; Daniel Nilsson ; Martin Engvall...
doi:10.3389/fneur.2023.1170005.s004.  , 2023
Link: https://doi.org/10.3389/..
 
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10

Genome sequencing with comprehensive variant calling identi..:

Marlene Ek ; Daniel Nilsson ; Martin Engvall...
https://www.frontiersin.org/articles/10.3389/fneur.2023.1170005/full.  , 2023
Link: https://doi.org/10.3389/..
 
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11

Table_2_Genome sequencing with comprehensive variant callin..:

Marlene Ek ; Daniel Nilsson ; Martin Engvall...
doi:10.3389/fneur.2023.1170005.s002.  , 2023
Link: https://doi.org/10.3389/..
 
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12

Table_1_Genome sequencing with comprehensive variant callin..:

Marlene Ek ; Daniel Nilsson ; Martin Engvall...
doi:10.3389/fneur.2023.1170005.s001.  , 2023
Link: https://doi.org/10.3389/..
 
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13

Table_3_Genome sequencing with comprehensive variant callin..:

Marlene Ek ; Daniel Nilsson ; Martin Engvall...
doi:10.3389/fneur.2023.1170005.s003.  , 2023
Link: https://doi.org/10.3389/..
 
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14

African Ancestry Analysis and Admixture Genetic Mapping for..:

Tandon, Arti ; Chen, Ching J ; Penman, Alan...
qt5wr5r194.  , 2015
Link: https://escholarship.org..
 
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