Naomi Meeks

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 11 papers. Top paper: “Automated syndrome diagnosis by three-dimensional facial imaging”.

Automated syndrome diagnosis by three-dimensional facial imaging

Genetics in Medicine(2020)10.1038/s41436-020-0845-y

N/A

0DataRank · unranked

106 citations

J. David Aponte, David C. Katz, Jordan J. Bannister, Sheri L. Riccardi, Nick Mahasuwan +33 more

Germline mutation in POLR2A: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100014

N/A

0DataRank · unranked

22 citations

Payal Arora, Michael M. Khayat, Leah J. Smith, Andrea M. Lewis, Linda Rossetti +19 more

Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12290

N/A

0DataRank · unranked

38 citations

Erik A. Eklund, Sergey A. Shiryaev, Yin Yao Dong, Mary‐Alice Abbott, Carla Asteggiano +48 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

Genome mapping resolves structural variation within segmental duplications associated with microdeletion/microduplication syndromes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.30.071449

N/A

0DataRank · unranked

2 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +6 more

Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation

Genetics(2021)10.1093/genetics/iyaa038

N/A

0DataRank · unranked

20 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +7 more

ClinGen’s Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Genetics in Medicine(2022)10.1016/j.gim.2022.02.019

N/A

0DataRank · unranked

13 citations

Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore, Kristy Lee, Christine M. Pak +17 more

Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors

Nature Communications(2024)10.1038/s41467-024-52095-x

N/A

0DataRank · unranked

9 citations

Daniel Woike, Daniel Greene, Sarada Das, Kevin Pfeifer, Weimin Yuan +53 more

Implementing evidence-based assertions of clinical actionability in the context of secondary findings: Updates from the ClinGen Actionability Working Group

Genetics in Medicine(2024)10.1016/j.gim.2024.101164

N/A

0DataRank · unranked

4 citations

Marian J. Gilmore, Joanna E. Bulkley, Pranesh Chakraborty, Orit Dagan‐Rosenfeld, Ann Katherine M. Foreman +21 more

The role of double heterozygotes of SLC3A1 and SLC7A9 in the prevalence of cystine stones

Genetics in Medicine(2024)10.1016/j.gim.2024.101281

N/A

0DataRank · unranked

1 citations

Ishita Patel, Katreya Lovrenert, Brian H. Eisner, Naomi Meeks, Anne Chun‐Hui Tsai +4 more

An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis

Mitochondrion(2024)10.1016/j.mito.2024.101973

N/A

0DataRank · unranked

2 citations

Austin Larson, Naomi Meeks, Sara Gracie, Marisa W. Friederich, Sommer Gaughan +9 more