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Chambert, Kimberly
109
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Online (109)
Mediatypes
Articles (Online) (24)
OpenAccess-fulltext (85)
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1
Genome-wide association study of school grades identifies g..:
Rajagopal, Veera M.
;
Ganna, Andrea
;
Coleman, Jonathan R. I.
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
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2
Exome sequencing in schizophrenia-affected parent–offspring..:
Howrigan, Daniel P.
;
Rose, Samuel A.
;
Samocha, Kaitlin E.
...
Nature Neuroscience. 23 (2020) 2 - p. 185-193 , 2020
Link:
https://doi.org/10.1038/..
?
3
Identification of common genetic risk variants for autism s..:
Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium
;
Grove, Jakob
;
Ripke, Stephan
...
Nature Genetics. 51 (2019) 3 - p. 431-444 , 2019
Link:
https://doi.org/10.1038/..
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4
Contribution of Rare Copy Number Variants to Bipolar Disord..:
Charney, Alexander W.
;
Stahl, Eli A.
;
Green, Elaine K.
...
Biological Psychiatry. 86 (2019) 2 - p. 110-119 , 2019
Link:
https://doi.org/10.1016/..
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5
Disentangling polygenic associations between attention-defi..:
Verhoef, Ellen
;
Demontis, Ditte
;
Burgess, Stephen
...
Translational Psychiatry. 9 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
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6
Su1089 - Presence of Bile Acids Detected in Human Saliva us..:
Perez, Nisha
;
Shao, James Z.
;
Mittleman, Robert
...
Gastroenterology. 154 (2018) 6 - p. S-484 , 2018
Link:
https://doi.org/10.1016/..
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7
Discovery of the first genome-wide significant risk loci fo..:
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
;
Demontis, Ditte
;
Walters, Raymond K.
...
Nature Genetics. 51 (2018) 1 - p. 63-75 , 2018
Link:
https://doi.org/10.1038/..
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8
Ultra-Rare Protein-Altering Variants Among 4,877 Swedish In..:
Genovese, Giulio
;
Fromer, Menachem
;
Stahl, Eli
...
European Neuropsychopharmacology. 27 (2017) - p. S426-S427 , 2017
Link:
https://doi.org/10.1016/..
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9
Damaging Missense De Novo Coding Mutations Contribute To Sc..:
Howrigan, Daniel
;
Samocha, Kaitlin
;
Kosmicki, Jack
...
European Neuropsychopharmacology. 27 (2017) - p. S427-S428 , 2017
Link:
https://doi.org/10.1016/..
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10
Mutation intolerant genes and targets of FMRP are enriched ..:
Leonenko, Ganna
;
Richards, Alexander L.
;
Walters, James T.
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 174 (2017) 7 - p. 724-731 , 2017
Link:
https://doi.org/10.1002/..
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11
Increased burden of ultra-rare protein-altering variants am..:
Genovese, Giulio
;
Fromer, Menachem
;
Stahl, Eli A
...
Nature Neuroscience. 19 (2016) 11 - p. 1433-1441 , 2016
Link:
https://doi.org/10.1038/..
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12
Evidence of Common Genetic Overlap Between Schizophrenia an..:
Hubbard, Leon
;
Tansey, Katherine E.
;
Rai, Dheeraj
...
Schizophrenia Bulletin. 42 (2015) 3 - p. 832-842 , 2015
Link:
https://doi.org/10.1093/..
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13
Novel Findings from CNVs Implicate Inhibitory and Excitator..:
Pocklington, Andrew J.
;
Rees, Elliott
;
Walters, James T.R.
...
Neuron. 86 (2015) 5 - p. 1203-1214 , 2015
Link:
https://doi.org/10.1016/..
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14
De novo CNVs in bipolar affective disorder and schizophreni:
Georgieva, Lyudmila
;
Rees, Elliott
;
Moran, Jennifer L.
...
Human Molecular Genetics. 23 (2014) 24 - p. 6677-6683 , 2014
Link:
https://doi.org/10.1093/..
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15
5:15 PM NOVEL GENETIC RISK VARIANTS FOR CLOZAPINE-ASSOCIATE..:
Legge, Sophie
;
Hamshere, Marian
;
Ripke, Stephan
...
Schizophrenia Research. 153 (2014) - p. S66-S67 , 2014
Link:
https://doi.org/10.1016/..
1-15