TH
Tertius Hough

Highly Cited

98
Works
4,420
Citations
34
H-Index
Search Authors
Author Statistics
  • OpenAlex ID A5001377483
  • i10-Index 46
  • 2-Yr Mean Citedness 0.00
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Tertius Hough

Also known as: Hough, T, Hough, Tertius Anton, T. Hough, Tertius A Hough, Tertius A. Hough

98

Total Works

4,420

Citations

34

H-Index

46

i10-Index

Citation & Works Trend by Year
25 years active
Top Research Topics
Parathyroid Disorders and Treatments (34) Genetic Mapping and Diversity in Plants and Animals (11) Genomics and Rare Diseases (8) Plant Genetic and Mutation Studies (8) Dermatological and Skeletal Disorders (8)
Recent Publications
15 shown
Year Publication Title Citations Action
2023 Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout The FASEB Journal 0
2023 A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X ( NFIX ) Gene Has Phenotypic Features of Marshall‐Smith Syndrome JBMR Plus 6
2023 Author response for "A mouse model with a frameshift mutation in the nuclear factor I/X ( NFIX ) gene has phenotypic features of Marshall‐Smith Syndrome" Publons reviews and discussion 0
2023 Author response for "A mouse model with a frameshift mutation in the nuclear factor I/X ( NFIX ) gene has phenotypic features of Marshall‐Smith Syndrome" Publons reviews and discussion 0
2022 Author Correction: EMPReSS: standardized phenotype screens for functional annotation of the mouse genome Nature Genetics 0
2021 Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes Disease Models & Mechanisms 35
2021 Chronically elevated branched chain amino acid levels are pro-arrhythmic Cardiovascular Research 64
2020 Human and mouse essentiality screens as a resource for disease gene discovery Nature Communications 105
2020 Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism Endocrine Connections 9
2019 A mouse model generated by CRISPR-Cas9 with a frameshift mutation in the nuclear factor 1/X (NFIX) gene has phenotypic features reported in Marshall-Smith Syndrome (MSS) patients Endocrine Abstracts 0
2019 Mice harbouring a germline heterozygous AP2S1 mutation, Arg15Leu, are a model for familial hypocalciuric hypercalcaemia type 3 (FHH3) Endocrine Abstracts 0
2019 Drug safety Africa: An overview of safety pharmacology & toxicology in South Africa Journal of Pharmacological and Toxicological Methods 2
2019 OR30-5 Germline Ablation of G-Protein Subunit Alpha-11 in Mice Causes Hypercalcemia That Is Rectified by Treatment with Cinacalcet Journal of the Endocrine Society 1
2019 MON-539 Mice Harboring a Germline Heterozygous AP2S1 Mutation, Arg15Leu, Are a Model for Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Journal of the Endocrine Society 1
2019 Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis Journal of Bone and Mineral Research 10

Data source: OpenAlex API