# Hana Lango Allen

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hana-lango-allen/

## Facts

| Field | Value |
| --- | --- |
| Citations | 27,728 |
| Field | Genetic Associations and Epidemiology |
| h-index | 52 |
| i10-index | 73 |
| Last Known Institution | University of Cambridge |
| OpenAlex ID | https://openalex.org/A5011793057 |
| ORCID iD | https://orcid.org/0000-0002-7803-8688 |
| Works | 106 |

## Researcher papers

- [A Common Variant in the <i>FTO</i> Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity](https://scholariq.org/papers/a-common-variant-in-the-i-fto-i-gene-is-associated-with-body-mass-index-and/)
- [Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index](https://scholariq.org/papers/association-analyses-of-249-796-individuals-reveal-18-new-loci-associated-with/)
- [Hundreds of variants clustered in genomic loci and biological pathways affect human height](https://scholariq.org/papers/hundreds-of-variants-clustered-in-genomic-loci-and-biological-pathways-affect/)
- [Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-data-and-large-scale-replication/)
- [Whole-genome sequencing of patients with rare diseases in a national health system](https://scholariq.org/papers/whole-genome-sequencing-of-patients-with-rare-diseases-in-a-national-health/)
- [Whole-genome sequencing of a sporadic primary immunodeficiency cohort](https://scholariq.org/papers/whole-genome-sequencing-of-a-sporadic-primary-immunodeficiency-cohort/)
- [Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans](https://scholariq.org/papers/loss-of-function-nuclear-factor-b-subunit-1-nfkb1-variants-are-the-most-common/)
- [An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy](https://scholariq.org/papers/an-in-frame-deletion-at-the-polymerase-active-site-of-pold1-causes-a-multisystem/)
- [Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations](https://scholariq.org/papers/characterization-of-the-clinical-and-immunologic-phenotype-and-management-of-157/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Diabetes and associated disorders](https://scholariq.org/topics/diabetes-and-associated-disorders/)

## Researcher university

- [University of Cambridge](https://scholariq.org/institutions/university-of-cambridge/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.