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                             13 results found
no title author magazine year volume issue page(s) type
1 Autism-specific PTEN p.Ile135Leu variant and an autism genetic background combine to dysregulate cortical neurogenesis Fu, Shuai

110 5 p. 826-845
article
2 Bi-allelic variants in INTS11 are associated with a complex neurological disorder Tepe, Burak

110 5 p. 774-789
article
3 De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis Timberlake, Andrew T.

110 5 p. 846-862
article
4 Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures Örd, Tiit

110 5 p. 722-740
article
5 Fast and accurate Bayesian polygenic risk modeling with variational inference Zabad, Shadi

110 5 p. 741-761
article
6 Genetic heritage of the Baphuthi highlights an over-ethnicized notion of “Bushman” in the Maloti-Drakensberg, southern Africa Daniels, Ryan Joseph

110 5 p. 880-894
article
7 Kurt Hirschhorn (1926–2022) Gelb, Bruce D.

110 5 p. 717-721
article
8 POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies Smallwood, Kelly

110 5 p. 809-825
article
9 Scalable mixed model methods for set-based association studies on large-scale categorical data analysis and its application to exome-sequencing data in UK Biobank Bi, Wenjian

110 5 p. 762-773
article
10 SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability Bogaert, Elke

110 5 p. 790-808
article
11 The functional impact of 1,570 individual amino acid substitutions in human OTC Lo, Russell S.

110 5 p. 863-879
article
12 This month in The Journal Spencer, Kylee L.

110 5 p. 715-716
article
13 Trio RNA sequencing in a cohort of medically complex children Deshwar, Ashish R.

110 5 p. 895-900
article
                             13 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands