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| 37509153 | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease Formation. | Biomolecules | 2023 |
| 37084271 | Predicting the pathogenicity of missense variants using features derived from AlphaFold2. | Bioinformatics | 2023 |
| 37169019 | Analysis of candidate genes for cleft lip ± cleft palate using murine single-cell expression data. | Front Cell Dev Biol | 2023 |
| 34528480 | MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration. | J Dent Res | 2022 |
| 35708486 | Novel genes and sex differences in COVID-19 severity. | Hum Mol Genet | 2022 |
| 35362267 | Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. | Birth Defects Res | 2022 |
| 35851378 | Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding. | Nat Biotechnol | 2022 |
| 37034418 | Systematic assays and resources for the functional annotation of non-coding variants. | Med Genet | 2022 |
| 36589413 | Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of <i>de novo</i> mutations. | HGG Adv | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 35923707 | Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. | Front Genet | 2022 |
| 36352089 | A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. | Commun Biol | 2022 |
| 35101171 | Genetic Predisposition and the Variable Course of Infectious Diseases. | Dtsch Arztebl Int | 2022 |
| 34889978 | Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity. | Hum Genet | 2022 |
| 34994518 | Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax. | Am J Med Genet A | 2022 |
| 35110662 | Allele-specific transcription factor binding in a cellular model of orofacial clefting. | Sci Rep | 2022 |
| 35199045 | First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>. | HGG Adv | 2022 |
| 33057169 | Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. | Mol Psychiatry | 2021 |
| 33758887 | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. | medRxiv | 2021 |
| 34946818 | Iron Deficiency Caused by Intestinal Iron Loss-Novel Candidate Genes for Severe Anemia. | Genes (Basel) | 2021 |
| 35047836 | Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate. | HGG Adv | 2021 |
| 34597274 | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. | J Clin Invest | 2021 |
| 34188222 | LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding. | Nat Biotechnol | 2021 |
| 34210994 | TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19. | NPJ Genom Med | 2021 |
| 34004033 | Extending the allelic spectrum at noncoding risk loci of orofacial clefting. | Hum Mutat | 2021 |
| 33436526 | Structure-guided multivalent nanobodies block SARS-CoV-2 infection and suppress mutational escape. | Science | 2021 |
| 32373937 | Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study. | Int J Epidemiol | 2020 |
| 32065501 | Nine newly identified individuals refine the phenotype associated with MYT1L mutations. | Am J Med Genet A | 2020 |
| 33172359 | A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. | Z Kinder Jugendpsychiatr Psychother | 2020 |
| 32710482 | Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. | Genet Epidemiol | 2020 |
| 32467233 | Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development. | Development | 2020 |
| 30638414 | Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. | Epigenomics | 2019 |
| 31817908 | Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility Gene. | Genes (Basel) | 2019 |
| 31891614 | Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data. | PLoS One | 2019 |
| 30741946 | Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. | Transl Psychiatry | 2019 |
| 30850703 | Deletions and loss-of-function variants in TP63 associated with orofacial clefting. | Eur J Hum Genet | 2019 |
| 31049400 | p63 establishes epithelial enhancers at critical craniofacial development genes. | Sci Adv | 2019 |
| 28926086 | Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate. | Clin Genet | 2018 |
| 30067744 | Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. | PLoS Genet | 2018 |
| 30379966 | Exome sequencing in large, multiplex bipolar disorder families from Cuba. | PLoS One | 2018 |
| 29498243 | Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample. | Birth Defects Res | 2018 |
| 29053389 | MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach. | J Dent Res | 2018 |
| 29134786 | Investigation of dominant and recessive inheritance models in genome-wide association studies data of nonsyndromic cleft lip with or without cleft palate. | Birth Defects Res | 2018 |
| 27834299 | Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing. | J Dent Res | 2017 |
| 33473741 | The complete mitochondrial genome of the 'solar-powered' sea slug <i>Plakobranchus</i> cf. <i>ocellatus</i> (Heterobranchia: Panpulmonata: Sacoglossa). | Mitochondrial DNA B Resour | 2017 |
| 28232668 | Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. | Nat Commun | 2017 |
| 28087736 | Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only. | Hum Mol Genet | 2017 |
| 28272115 | Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety. | Psychiatr Genet | 2017 |
| 29045907 | Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy. | Immunity | 2017 |