Julie Hoover‐Fong

Also affiliated with Johns Hopkins Medicine, Green Chemistry

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 7 papers. Top paper: “The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities”.

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

The American Journal of Human Genetics(2015)10.1016/j.ajhg.2015.06.009

N/A

0.980DataRank · unranked

687 citations

Kati J. Buckingham, Shalini N. Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D. Smith +46 more

Prevalence of Hearing Loss and Hearing Aid Use Among US Medicare Beneficiaries Aged 71 Years and Older

JAMA Network Open(2023)10.1001/jamanetworkopen.2023.26320

N/A

0.732DataRank · unranked

131 citations

Emmanuel E. Garcia Morales, Clarice Myers, Alison Huang, Joshua R. Ehrlich, Olivia J. Killeen +7 more

Not just a carrier: Clinical presentation and management of patients with heterozygous disease‐causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.2056

N/A

0DataRank · unranked

14 citations

Katelynn G. Sagaser, Cathleen Lawson, Christine Hertenstein, Ashley Jachens, Katherine R. Forster +5 more

Body composition, anthropometry, and resting energy expenditure in adults with achondroplasia: a pilot study to determine best practices

Orphanet Journal of Rare Diseases(2025)10.1186/s13023-025-03912-z

N/A

0DataRank · unranked

0 citations

John McGready, Bobbie J. Henry-Barron, Celide Koerner, Julie Hoover‐Fong, Kerry Schulze

Growth Standards for Children With Smith–Magenis Syndrome ( SMS )

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64167

N/A

0DataRank · unranked

0 citations

John McGready, Leah Fleming, Kerry Schulze, Folami Duncan, Alexis Leonard +6 more

Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome

PLoS Genetics(2022)10.1371/journal.pgen.1010504

N/A

0DataRank · unranked

14 citations

Renan Paulo Martin, Elizabeth Wohler, Elizabeth Partan, Elizabeth Walek, Shaima Salman +13 more

Mapping the Relationship between Dysmorphology and Cognitive, Behavioral, and Developmental Outcomes in Children with Autism Spectrum Disorder

Autism Research(2020)10.1002/aur.2314

N/A

0DataRank · unranked

6 citations

Lisa D. Wiggins, Laura A. Schieve, Marshalyn Yeargin‐Allsopp, Patricia M. Dietz, Arthur S. Aylsworth +10 more