Bocher, Ozvan
32  Ergebnisse:
Personensuche X
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1

Multi-ancestry genome-wide study in >2.5 million individual..:

Suzuki, Ken ; Hatzikotoulas, Konstantinos ; Southam, Lorraine...
VA Million Veteran Program , AMED GRIFIN Diabetes Initiative Japan , BioBank Japan Project , Penn Medicine BioBank , Regeneron Genetics Center , eMERGE Consortium , International Consortium for Blood Pressure (ICBP) , Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) , Suzuki , K , Hatzikotoulas , K , Southam , L , Taylor , H J , Yin , X , Lorenz , K M , Mandla , R , Huerta-Chagoya , A , Rayner , N W , Bocher , O , Ana Luiza de , S V A , Sonehara , K , Namba , S , Lee , S S K , Preuss , M H , Petty , L E , Schroeder , P , Vanderwerff , B , Kals , M , Bragg , F , Lin , K , Guo , X , Zhang , W , Yao , J , Kim , Y J , Graff , M , Takeuchi , F , Nano , J , Lamri , A , Nakatochi , M , Moon , S , Scott , R A , Cook , J P , Lee , J-J , Pan , I , Taliun , D , Parra , E J , Chai , J-F , Bielak , L F , Tabara , Y , Hai , Y , Thorleifsson , G , Grarup , N , Sofer , T , Chen , W-M , Prins , B P , Kamali , Z , Huang , W , Zhang , L , Wang , Y-X , Morris , A P ....  , 2023
 
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5

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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6

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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7

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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9

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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10

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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11

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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12

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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13

Testing for association with rare variants in the coding an..:

Bocher, Ozvan ; Ludwig, Thomas E ; Oglobinsky, Marie-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009923.  , 2022
 
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14

Whole exome sequencing, a hypothesis-free approach to inves..:

Gourhant, Lenaick ; Bocher, Ozvan ; de Saint Martin, Luc...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.rbmo.2021.01.008.  , 2021
 
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15

Whole exome sequencing, a hypothesis-free approach to inves..:

Gourhant, Lenaick ; Bocher, Ozvan ; de Saint Martin, Luc...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.rbmo.2021.01.008.  , 2021
 
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