Charlotte A. Hobbs

MedicineBiochemistry, Genetics and Molecular Biology

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 4%percentile

0.752Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

Genome Medicine(2023)10.1186/s13073-023-01166-7

Top 27%

0.752DataRank

Top 27%29 citations

Edgar J. Hernández, Charlotte A. Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin F. Juarez +9 more

Papers

Driven by 30 papers — median percentile 37. Top paper: “Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission”.

Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission

Nature(2022)10.1038/s41586-022-05049-6

N/A

0.939DataRank · unranked

523 citations

Joshua I. Levy, Peter De Hoff, Greg Humphrey, Amanda Birmingham, Kristen Jepsen +95 more

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

Genome Medicine(2023)10.1186/s13073-023-01166-7

Top 27%

0.752DataRank

Top 27%29 citations

Edgar J. Hernández, Charlotte A. Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin F. Juarez +9 more

Circular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastoma

Nature Genetics(2023)10.1038/s41588-023-01551-3

N/A

0.631DataRank · unranked

66 citations

Jens Luebeck, Sunita Sridhar, Ivy Tsz-Lo Wong, Deobrat Dixit, Shanqing Wang +43 more

A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62759

N/A

0.417DataRank · unranked

9 citations

Mario A. Cleves, Gary M. Shaw, Wendy N. Nembhard, Eirini Nestoridi, Mary M. Jenkins +11 more

Integrated Genomic and Social Network Analyses of SARS-CoV-2 Transmission in the Healthcare Setting

Clinical Infectious Diseases(2024)10.1093/cid/ciad738

N/A

0.312DataRank · unranked

7 citations

Shira R. Abeles, Chris Longhurst, Lucy E. Horton, Frank Edward Myers, Lindsay Riggs-Rodriguez +58 more

Exome sequencing identifies variants in infants with sacral agenesis

Birth Defects Research(2022)10.1002/bdr2.1987

N/A

0.241DataRank · unranked

4 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +21 more

Response to Grosse et al.

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.004

N/A

0.104DataRank · unranked

1 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson +46 more

Emergence of an early SARS-CoV-2 epidemic in the United States

medRxiv(2021)10.1101/2021.02.05.21251235

N/A

0DataRank · unranked

10 citations

Karthik Gangavarapu, Catelyn Anderson, Allison R. Smither, John A. Vanchiere, Rebecca Rose +47 more

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00206-8

N/A

0DataRank · unranked

6 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00205-9

N/A

0DataRank · unranked

5 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.003

N/A

0DataRank · unranked

171 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson +46 more

Approaches to long-read sequencing in a clinical setting to improve diagnostic rate

Scientific Reports(2022)10.1038/s41598-022-20113-x

N/A

0DataRank · unranked

56 citations

Serge Batalov, Aaron M. Wenger, Christine Lambert, Harsharan Dhillon, Richard Hall +8 more

Differential newborn DNA methylation among individuals with complex congenital heart defects and childhood lymphoma

Birth Defects Research(2022)10.1002/bdr2.2105

N/A

0DataRank · unranked

2 citations

Wei Yang, Pagna Sok, Ming Li, Suzan L. Carmichael, Julie Von Behren +8 more

3D genome mapping identifies subgroup-specific chromosome conformations and tumor-dependency genes in ependymoma

Nature Communications(2023)10.1038/s41467-023-38044-0

N/A

0DataRank · unranked

26 citations

Aylin Camgöz, Owen Chapman, Sameena Wani, Donglim Esther Park, Jens-Martin Hübner +46 more

Safer at school early alert: an observational study of wastewater and surface monitoring to detect COVID-19 in elementary schools

The Lancet Regional Health - Americas(2023)10.1016/j.lana.2023.100449

N/A

0DataRank · unranked

40 citations

Smruthi Karthikeyan, Tommi Gaines, Richard S. Garfein, Rodolfo A. Salido, Victor Cantu +66 more

Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63363

N/A

0DataRank · unranked

11 citations

Lucia Guidugli, Monia Hammer, Chelsea Barrows, Anne Gregor, Sangmoon Lee +9 more

The Genomic landscape of short tandem repeats across multiple ancestries

PLoS ONE(2023)10.1371/journal.pone.0279430

N/A

0DataRank · unranked

8 citations

Serge Batalov, Yan Ding, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock +3 more

A gene‐based association test of interactions for maternal–fetal genotypes identifies genes associated with nonsyndromic congenital heart defects

Genetic Epidemiology(2023)10.1002/gepi.22533

N/A

0DataRank · unranked

3 citations

Chen Lyu, Nianjun Liu, Wendy N. Nembhard, John S. Witte, Charlotte A. Hobbs +3 more

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101851

N/A

0DataRank · unranked

4 citations

Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai +72 more

Exome sequencing identifies variants in infants with sacral agenesis

UNC Libraries(2024)10.17615/sevc-bn40

N/A

0DataRank · unranked

0 citations

Faith Pangilinan, Andrew F. Olshan, Richard H. Finnell, Martha M. Werler, Cynthia A. Moore +24 more

A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

UNC Libraries(2024)10.17615/ph8v-yc50

N/A

0DataRank · unranked

0 citations

Mary M. Jenkins, Sara R. Rashkin, Paul A. Romitti, Andrew F. Olshan, Marilyn L. Browne +11 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

UNC Libraries(2024)10.17615/4645-7p40

N/A

0DataRank · unranked

0 citations

Marcia L. Feldkamp, Nathan Pankratz, Lawrence C. Brody, John W. Lane, K.M. Conway +18 more

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.003

N/A

0DataRank · unranked

191 citations

Michelle M. Clark, Mary Gaughran, Julie A. Cakici, Sara Caylor, Christina Clarke +62 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

UNC Libraries(2024)10.17615/4h14-yj71

N/A

0DataRank · unranked

0 citations

Jianlin Li, Paul A. Romitti, Wendy N. Nembhard, Andrew F. Olshan, Marilyn L. Browne +11 more

Neural tube defects and maternal intake of micronutrients related to one-carbon metabolism or antioxidant activity

UNC Libraries(2020)10.17615/qc5d-ec05

N/A

0DataRank · unranked

0 citations

Gary M. Shaw, Yan Qi, Mark A. Canfield, R. J. Berry, Bridget Mosley +3 more

The national birth defects prevention study: A review of the methods: NBDPS METHODS REVIEW

UNC Libraries(2020)10.17615/w46z-wa53

Top 100%

0DataRank

Top 100%0 citations

Marilyn L. Browne, Marcia L. Feldkamp, Suzanne M. Gilboa, Gary M. Shaw, Charlotte A. Hobbs +10 more

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00192-x

N/A

0DataRank · unranked

76 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Emergence of an early SARS-CoV-2 epidemic in the United States

Cell(2021)10.1016/j.cell.2021.07.030

N/A

0DataRank · unranked

52 citations

Karthik Gangavarapu, Catelyn Anderson, Allison R. Smither, John A. Vanchiere, Rebecca Rose +47 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62439

N/A

0DataRank · unranked

8 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +17 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

PLoS Genetics(2021)10.1371/journal.pgen.1009413

N/A

0DataRank · unranked

4 citations

Emine Bircan, Xinyu Tang, Mohammed S. Orloff, Charlotte A. Hobbs, Marilyn L. Browne +11 more

Charlotte A. Hobbs

Indexed papers

Top data-sharing exemplar

Papers