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UK10K Consortium
104  results:
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1

Steroid receptor coactivator-1 modulates the function of Po..:

Yang, Yongjie ; van der Klaauw, Agatha A. ; Zhu, Liangru...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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2

GARFIELD classifies disease-relevant genomic features throu..:

UK10K Consortium ; Iotchkova, Valentina ; Ritchie, Graham R. S....
Nature Genetics.  51 (2019)  2 - p. 343-353 , 2019
Link: https://doi.org/10.1038/..
 
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3

Bi-allelic mutations in MYL1 cause a severe congenital myop..:

Ravenscroft, Gianina ; Zaharieva, Irina ; Bortolotti, Carlo A...
Human Molecular Genetics.  , 2018
Link: https://doi.org/10.1093/..
 
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4

Author Correction: Discovery and refinement of genetic loci..:

UK10K Consortium ; Iotchkova, Valentina ; Huang, Jie...
Nature Genetics.  50 (2018)  12 - p. 1752-1752 , 2018
Link: https://doi.org/10.1038/..
 
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5

The contribution of rare variants to risk of schizophrenia ..:

INTERVAL Study ; Singh, Tarjinder ; Walters, James T R...
Nature Genetics.  49 (2017)  8 - p. 1167-1173 , 2017
Link: https://doi.org/10.1038/..
 
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6

Erratum: Corrigendum: Mutations in the histone methyltransf..:

UK10K Consortium ; Meyer, Esther ; Carss, Keren J...
Nature Genetics.  49 (2017)  6 - p. 969-969 , 2017
Link: https://doi.org/10.1038/..
 
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7

Mutations in the histone methyltransferase gene KMT2B cause..:

UK10K Consortium ; Meyer, Esther ; Carss, Keren J...
Nature Genetics.  49 (2016)  2 - p. 223-237 , 2016
Link: https://doi.org/10.1038/..
 
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8

Discovery and refinement of genetic loci associated with ca..:

UK10K Consortium ; Iotchkova, Valentina ; Huang, Jie...
Nature Genetics.  48 (2016)  11 - p. 1303-1312 , 2016
Link: https://doi.org/10.1038/..
 
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9

A secreted WNT-ligand-binding domain of FZD5 generated by a..:

Liu, Chunqiao ; Widen, Sonya A. ; Williamson, Kathleen A....
Human Molecular Genetics.  25 (2016)  7 - p. 1382-1391 , 2016
Link: https://doi.org/10.1093/..
 
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10

A method for analyzing multiple continuous phenotypes in ra..:

UK10K Consortium ; Sun, Jianping ; Oualkacha, Karim...
European Journal of Human Genetics.  24 (2016)  9 - p. 1344-1351 , 2016
Link: https://doi.org/10.1038/..
 
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11

An interactive genome browser of association results from t..:

Geihs, Matthias ; Yan, Ying ; Walter, Klaudia...
Bioinformatics.  31 (2015)  24 - p. 4029-4031 , 2015
Link: https://doi.org/10.1093/..
 
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12

Timing, rates and spectra of human germline mutation:

UK10K Consortium ; Rahbari, Raheleh ; Wuster, Arthur...
Nature Genetics.  48 (2015)  2 - p. 126-133 , 2015
Link: https://doi.org/10.1038/..
 
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13

Targeted Next‐Generation Sequencing Analysis of 1,000 Indiv..:

Grozeva, Detelina ; Carss, Keren ; Spasic‐Boskovic, Olivera...
Human Mutation.  36 (2015)  12 - p. 1197-1204 , 2015
Link: https://doi.org/10.1002/..
 
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14

The UK10K project identifies rare variants in health and di..:

The UK10K Consortium ; Walter, Klaudia ; Min, Josine L....
Nature.  526 (2015)  7571 - p. 82-90 , 2015
Link: https://doi.org/10.1038/..
 
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15

Height-reducing variants and selection for short stature in..:

UK10K Consortium ; Zoledziewska, Magdalena ; Sidore, Carlo...
Nature Genetics.  47 (2015)  11 - p. 1352-1356 , 2015
Link: https://doi.org/10.1038/..
 
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