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PubPharm (110)
1
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations
enthalten in:
Nature medicine
| 2024
von
Lennon, N.
|
Kottyan, L.
|
Kachulis, C.
| +79
UpdateOf: medRxiv. 2023 Jun 05;:. - PMID 37333246
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2
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
enthalten in:
Genome medicine
| 2024
von
Puckelwartz, M.
|
Pesce, L.
|
Hernandez, E.
| +20
UpdateOf: medRxiv. 2023 Mar 29;:. - PMID 37034657
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3
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
enthalten in:
Genome medicine
| 2024
von
Puckelwartz, M.
|
Pesce, L.
|
Hernandez, E.
| +20
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4
Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations
enthalten in:
bioRxiv.org
| 2023
von
Lennon, N.
|
Kottyan, L.
|
Kachulis, C.
| +73
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5
Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Lennon, N.
|
Kottyan, L.
|
Kachulis, C.
| +75
UpdateIn: Nat Med. 2024 Feb;30(2):480-487. - PMID 38374346
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6
Emerging Activity Patterns and Synaptogenesis in Dissociated Hippocampal Cultures
enthalten in:
bioRxiv.org
| 2023
von
Suresh, J.
|
Saddler, M.
|
Bindokas, V.
| +5
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7
Emerging Activity Patterns and Synaptogenesis in Dissociated Hippocampal Cultures
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Suresh, J.
|
Saddler, M.
|
Bindokas, V.
| +5
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8
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
enthalten in:
bioRxiv.org
| 2023
von
Puckelwartz, M.
|
Pesce, L.
|
Hernandez, E.
| +19
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9
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Puckelwartz, M.
|
Pesce, L.
|
Hernandez, E.
| +19
UpdateIn: Genome Med. 2024 Jan 16;16(1):13. - PMID 38229148
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10
Opposing effects of genetic variation in MTCH2 for obesity versus heart failure
enthalten in:
Human molecular genetics
| 2023
von
Fischer, J.
|
Monroe, T.
|
Pesce, L.
| +7
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