Pub ID | Title | Author(s) | Year | Journal |
14435 | A comprehensive spatio-cellular map of the human hypothalamus | John A. Tadross (+16) | 2025 | Nature |
12198 | Characterization of dominant-negative growth hormone receptor variants reveals a potential therapeutic target for short stature | Afiya Andrews (+10) | 2023 | European Journal of Endocrinology |
10819 | Damaging missense variants in IGF1R implicate a role for IGF-1 resistance in the etiology of type 2 diabetes | Eugene J. Gardner (+11) | 2022 | Cell Genomics |
13442 | Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health | Sam M. Lockhart (+41) | 2024 | Nature Metabolism |
14741 | Deleterious variants in intolerant genes reveal new candidates for self-limited delayed puberty | Raíssa C Rezende (+24) | 2025 | European Journal of Endocrinology |
14012 | Detection and characterization of male sex chromosome abnormalities in the UK Biobank study | Yajie Zhao (+19) | 2022 | Genetics in Medicine |
8547 | Elucidating the genetic basis of social interaction and isolation | Felix R. Day (+2) | 2018 | Nature Communications |
8738 | Genetic determinants of micronucleus formation in vivo | D. J. Adams (+43) | 2024 | Nature |
13506 | Genetic links between ovarian ageing, cancer risk and de novo mutation rates | Stasa Stankovic (+34) | 2024 | Nature |
7540 | Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility | Daniel J Wright (+18) | 2017 | Nature Genetics |
11163 | Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus | Iain Mathieson (+120) | 2023 | Nature Human Behaviour |
8523 | Genome-wide association study for risk taking propensity indicates shared pathways with body mass index | Emma A. D. Clifton (+9) | 2018 | Communications Biology |
12694 | Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour | Bastiaan T. Heijmans (+63) | 2021 | Nature Human Behaviour |
12647 | Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution | Mine Koprulu (+29) | 2021 | The Journal of Clinical Endocrinology & Metabolism |
10207 | Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesity | Lena R Kaisinger (+17) | 2023 | Cell Genomics |
13096 | Likely causal effects of insulin resistance and IGF-1 bioaction on childhood and adult adiposity: a Mendelian randomization study | Duaa I. Olwi (+9) | 2024 | International Journal of Obesity |
11772 | Loss of transient receptor potential channel 5 causes obesity and postpartum depression | Yongxiang Li (+34) | 2024 | Cell |
9211 | Observational and genetic associations between cardiorespiratory fitness and cancer: a UK Biobank and international consortia study | Eleanor L. Watts (+22) | 2023 | British Journal of Cancer |
11585 | Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency | Saleh Shekari (+18) | 2023 | Nature Medicine |
13383 | Population-Based Study of Rare Coding Variants in NR5A1/SF-1 | Chrysanthi Kouri (+6) | 2024 | Journal of the Endocrine Society |
11578 | Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and Puberty | Katie Duckett (+35) | 2023 | The Journal of Clinical Endocrinology & Metabolism |
9968 | Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease | Yajie Zhao (+33) | 2024 | Nature Genetics |
9217 | Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation | Elizabeth J. Radford (+18) | 2023 | Nature Communications |
9605 | Shared and distinct genetic etiologies for different types of clonal hematopoiesis | Derek W. Brown (+14) | 2023 | Nature Communications |
11751 | Understanding the genetic complexity of puberty timing across the allele frequency spectrum | Katherine A. Kentistou (+219) | 2024 | Nature Genetics |