Amber Hildreth

1.2k total citations · 1 hit paper
10 papers, 327 citations indexed

About

Amber Hildreth is a scholar working on Genetics, Surgery and Epidemiology. According to data from OpenAlex, Amber Hildreth has authored 10 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Surgery and 3 papers in Epidemiology. Recurrent topics in Amber Hildreth's work include Genomics and Rare Diseases (3 papers), Liver Disease Diagnosis and Treatment (2 papers) and Pediatric Hepatobiliary Diseases and Treatments (2 papers). Amber Hildreth is often cited by papers focused on Genomics and Rare Diseases (3 papers), Liver Disease Diagnosis and Treatment (2 papers) and Pediatric Hepatobiliary Diseases and Treatments (2 papers). Amber Hildreth collaborates with scholars based in United States. Amber Hildreth's co-authors include Stephen F. Kingsmore, David Dimmock, Shimul Chowdhury, Shareef Nahas, Michelle M. Clark, Robert H. Kaplan, Jennifer Friedman, Matthew N. Bainbridge, Julie A. Cakici and Richard Kronick and has published in prestigious journals such as SHILAP Revista de lepidopterología, Drug Metabolism and Disposition and Inflammatory Bowel Diseases.

In The Last Decade

Amber Hildreth

9 papers receiving 321 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Amber Hildreth et al. npj Genomic Medicine profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Amber Hildreth United States	5	249	105	54	46	37	10	327
Wendy Benson United States	5	271 1.1×	110 1.0×	57 1.1×	48 1.0×	44 1.2×	10	341
Kalotina Machini United States	9	370 1.5×	109 1.0×	74 1.4×	53 1.2×	111 3.0×	15	518
Rebekah Jobling Canada	10	196 0.8×	266 2.5×	21 0.4×	53 1.2×	44 1.2×	24	550
Fernanda Caroline Soardi Brazil	13	171 0.7×	324 3.1×	17 0.3×	27 0.6×	9 0.2×	28	421
J. L. Chaussain France	7	92 0.4×	212 2.0×	20 0.4×	60 1.3×	22 0.6×	11	321
Mabel Yau United States	11	124 0.5×	239 2.3×	15 0.3×	145 3.2×	33 0.9×	36	396
Susan Rojahn United States	8	137 0.6×	79 0.8×	19 0.4×	18 0.4×	33 0.9×	13	263
Kathryn E. Hatchell United States	10	207 0.8×	124 1.2×	79 1.5×	14 0.3×	82 2.2×	40	402
Rita Bertalan Hungary	10	141 0.6×	187 1.8×	8 0.1×	27 0.6×	21 0.6×	23	328
Aida I. Al‐Aqeel Saudi Arabia	9	43 0.2×	55 0.5×	68 1.3×	22 0.5×	10 0.3×	17	200

Countries citing papers authored by Amber Hildreth

Since Specialization

Citations

This map shows the geographic impact of Amber Hildreth's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Amber Hildreth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amber Hildreth more than expected).

Fields of papers citing papers by Amber Hildreth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amber Hildreth. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Amber Hildreth. The network helps show where Amber Hildreth may publish in the future.

Co-authorship network of co-authors of Amber Hildreth

This figure shows the co-authorship network connecting the top 25 collaborators of Amber Hildreth. A scholar is included among the top collaborators of Amber Hildreth based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amber Hildreth. Amber Hildreth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Lee, Pei‐Shan, et al.. (2023). A neonatal case of vascular ring with Alagille syndrome. SHILAP Revista de lepidopterología. 11. 2050313X231197321–2050313X231197321. 1 indexed citations

2.

Hildreth, Amber, et al.. (2023). Distinguishing Autoimmune Hepatitis From Steatohepatitis in Adolescents With Obesity and Positive Screening Alanine Aminotransferase. JPGN Reports. 4(2). e292–e292. 3 indexed citations

3.

Thompson, Whitney S., Jacob R. Greenmyer, Brendan C. Lanpher, et al.. (2022). Ultra‐rapid whole genome sequencing: A paradigm shift in the pre‐transplant evaluation of neonatal acute liver failure. Liver Transplantation. 29(1). 118–121. 4 indexed citations

4.

Slowik, Voytek, Amber Hildreth, M. Cristina Pacheco, et al.. (2020). Hepatopulmonary Syndrome in an Adolescent With Insidious Hypoxia and Small Intrahepatic Portal Venous Shunts: Posttransplant Benefit From Sildenafil. Pediatric and Developmental Pathology. 23(6). 467–471.

5.

Hildreth, Amber, Mark A. Valasek, Irene Thung, et al.. (2018). Biallelic Mismatch Repair Deficiency in an Adolescent Female. SHILAP Revista de lepidopterología. 2018. 1–5. 3 indexed citations

6.

Farnaes, Lauge, Amber Hildreth, Nathaly M. Sweeney, et al.. (2018). Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization. npj Genomic Medicine. 3(1). 10–10. 280 indexed citations breakdown →

7.

Hildreth, Amber, Kristen Wigby, Shimul Chowdhury, et al.. (2017). Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann–Pick type C1 disease in a 7-week-old male with cholestasis. Molecular Case Studies. 3(5). a001966–a001966. 9 indexed citations

8.

Shakhnovich, Valentina, Carrie A. Vyhlidal, Craig A. Friesen, et al.. (2016). Decreased Pregnane X Receptor Expression in Children with Active Crohn’s Disease. Drug Metabolism and Disposition. 44(7). 1066–1069. 21 indexed citations

9.

Shakhnovich, Valentina, Darrell L. Dinwiddie, Amber Hildreth, Thomas M. Attard, & Stephen F. Kingsmore. (2014). A Novel Compound‐Heterozygous Epithelial Cell Adhesion Molecule Mutation in Tufting Enteropathy. Journal of Pediatric Gastroenterology and Nutrition. 64(1). e14–e16. 5 indexed citations

10.

Shakhnovich, Valentina, Carrie A. Vyhlidal, Craig A. Friesen, et al.. (2013). P-209 YI Decreased Pregnane X Receptor (PXR) Expression in Inflamed Versus Non-Inflamed Small Bowel of Children with Crohn’s Disease. Inflammatory Bowel Diseases. 19. S108–S109. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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