Caleb Bupp

Biochemistry, 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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 27 papers. Top paper: “High-Density Blood Transcriptomics Reveals Precision Immune Signatures of SARS-CoV-2 Infection in Hospitalized Individuals”.

High-Density Blood Transcriptomics Reveals Precision Immune Signatures of SARS-CoV-2 Infection in Hospitalized Individuals

Frontiers in Immunology(2021)10.3389/fimmu.2021.694243

N/A

1.1DataRank · unranked

43 citations

Nicholas Hartog, Dave Chesla, William E. Faber, Chanise P. Love, Rachid Karam +25 more

Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships

Genes(2023)10.3390/genes14010222

N/A

0.545DataRank · unranked

9 citations

Daniel T. Rasicci, David A. Hinds, Jackson T. Mitchell, Jacob K. Zieba, Joshua Mills +27 more

CCR5 and Biological Complexity: The Need for Data Integration and Educational Materials to Address Genetic/Biological Reductionism at the Interface of Ethical, Legal, and Social Implications

Frontiers in Immunology(2021)10.3389/fimmu.2021.790041

N/A

0.489DataRank · unranked

12 citations

Michèle Morris, Rama Shankar, Rosemary Olivero, Leah Buck, Cynthia L. Stenger +14 more

Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling

Genetics in Medicine(2022)10.1016/j.gim.2022.07.005

N/A

0.477DataRank · unranked

23 citations

Rachel VanCoillie, Elizabeth VanSickle, Deanna Alexis Carere, Kara Withrow, Erin Torti +43 more

The complex, dynamic SpliceOme of the small GTPase transcripts altered by technique, sex, genetics, tissue specificity, and RNA base editing

Frontiers in Cell and Developmental Biology(2022)10.3389/fcell.2022.1033695

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0.460DataRank · unranked

9 citations

Emily C. Sherry, Robert M. Vaughan, Marian L. Henderson, Jacob K. Zieba, Katie Uhl +9 more

Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglement

American Journal of Physiology-Cell Physiology(2025)10.1152/ajpcell.00749.2024

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0.165DataRank · unranked

2 citations

Surya B. Chhetri, Jackson T. Mitchell, Gage O. Leighton, Vladislav Jdanov, Jacob K. Zieba +35 more

Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans

Genetics in Medicine(2021)10.1016/j.gim.2021.09.014

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0DataRank · unranked

19 citations

Irena Feng, Ana Rita Costa, Rita Pinto‐Costa, Jennifer E. Neil, Oana Caluseriu +21 more

Emerging Role of ODC1 in Neurodevelopmental Disorders and Brain Development

Genes(2021)10.3390/genes12040470

N/A

0DataRank · unranked

32 citations

Caleb Bupp, Austin Frisch, Stephanie M. Bilinovich, Jerry L. Campbell, Daniel Vogt +6 more

Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype

Genetics in Medicine(2021)10.1016/j.gim.2021.09.005

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0DataRank · unranked

25 citations

Frédéric Ebstein, Anna Hurst, Marie Vincent, Ingrid Bader, Natasha L. Rudy +46 more

Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis

American Journal of Physiology-Lung Cellular and Molecular Physiology(2021)10.1152/ajplung.00440.2020

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0DataRank · unranked

14 citations

Mara L. Leimanis, Marie Adams, André S. Bachmann, Katie Uhl, Caleb Bupp +9 more

N‐methyl‐d‐aspartate (NMDA) receptor genetics: The power of paralog homology and protein dynamics in defining dominant genetic variants

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62554

N/A

0DataRank · unranked

3 citations

Angel Hernandez, Stephanie M. Bilinovich, Daniel Vogt, Laura Bedinger, Laurie H. Seaver +6 more

Profiling systemic physiology through blood‐based multidimensional RNAseq

The FASEB Journal(2021)10.1096/fasebj.2021.35.s1.03868

N/A

0DataRank · unranked

0 citations

Mara L. Leimanis, Dave Chesla, Caleb Bupp, Nicholas Hartog, Surender Rajasekaran +1 more

Variants in ADD1 Cause Intellectual Disability, Corpus Callosum Dysgenesis, and Ventriculomegaly in Humans

SSRN Electronic Journal(2021)10.2139/ssrn.3931622

N/A

0DataRank · unranked

0 citations

Irena Feng, Ana Rita Costa, Rita Pinto‐Costa, Jennifer Neil, Oana Caluseriu +16 more

Understanding patient‐level immune response to COVID‐19 can inform treatment options

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r4198

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0DataRank · unranked

0 citations

Austin Frisch, Nicholas Hartog, Caleb Bupp, Surender Rajasekaran, Jeremy W. Prokop

Two New Cases of Bachmann–Bupp Syndrome Identified through the International Center for Polyamine Disorders

Medical Sciences(2023)10.3390/medsci11020029

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0DataRank · unranked

7 citations

Elizabeth VanSickle, Marlie Vipond, Abby Dalman, Jeremy W. Prokop, Charles E. Schwartz +9 more

Understanding Insulin in the Age of Precision Medicine and Big Data: Under-Explored Nature of Genomics

Biomolecules(2023)10.3390/biom13020257

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0DataRank · unranked

8 citations

Amy M. Wilstermann, Jackson T. Mitchell, Nicholas E. Arnold, Surender Rajasekaran, Caleb Bupp +2 more

Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2025)10.1002/ajmg.c.32138

N/A

0DataRank · unranked

2 citations

Elizabeth VanSickle, Julianne Michael, Chad R. Schultz, Kelly Nguyen, Melissa Hoefer +3 more

Monitoring ODC activity and polyamines in Bachmann-Bupp syndrome patient biological samples

Methods in enzymology on CD-ROM/Methods in enzymology(2025)10.1016/bs.mie.2025.01.071

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0DataRank · unranked

1 citations

Elizabeth VanSickle, Caleb Bupp, André S. Bachmann, Chad R. Schultz

From castaways to discoveries: unveiling treasures in skin RNAseq using a novel multidimensional data processing workflow including infection-host dynamics

Physiological Genomics(2025)10.1152/physiolgenomics.00093.2024

N/A

0DataRank · unranked

1 citations

Alec Labadie, Rebecca L Hanson-Rios-Stutz, Austin Goodyke, Ella M. Moses, Akansha Das +18 more

Collection, preparation, and biobanking of clinical specimens for analysis in polyaminopathies

Methods in enzymology on CD-ROM/Methods in enzymology(2025)10.1016/bs.mie.2025.01.073

N/A

0DataRank · unranked

0 citations

Chad R. Schultz, André S. Bachmann, Caleb Bupp, Elizabeth VanSickle

Genomic, transcriptomic, and protein landscape profile of CFTR and cystic fibrosis

Human Genetics(2020)10.1007/s00439-020-02211-w

N/A

0DataRank · unranked

12 citations

James M.J. Lawlor, Xiaopeng Li, John Schuen, Susan L. Millard, Xi Zhang +11 more

Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity

Function(2025)10.1152/function.019.2025

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0DataRank · unranked

0 citations

Stephanie M. Bilinovich, Ember Tokarski, Sangeetha Vishweswaraiah, Sophie Vanderweele, Akansha Das +26 more

Intragenic Deletions of GNAS in Pseudohypoparathyroidism Type 1A Identify a New Region Affecting Methylation of Exon A/B

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa286

N/A

0DataRank · unranked

9 citations

Caleb Bupp, Michael March, Håkon Håkonarson, Michael A. Levine, Dong Li

SARS-CoV2 (COVID-19) Structural/Evolution Dynamicome: Insights into functional evolution and human genomics

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.15.098616

N/A

0DataRank · unranked

11 citations

Jacob Charron, Cynthia L. Stenger, Jared Painter, Hunter Steward, Taylor W. Cook +17 more

Disruption of RFX family transcription factors causes autism, attention deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

medRxiv(2020)10.1101/2020.09.09.20187104

N/A

0DataRank · unranked

9 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +71 more

Rapid whole-genome sequencing identifies a homozygous novel variant, His540Arg, in HSD17B4 resulting in D-bifunctional protein deficiency disorder diagnosis

Molecular Case Studies(2020)10.1101/mcs.a005496

N/A

0DataRank · unranked

7 citations

Stacie D. Adams, Kiely N. James, Shimul Chowdhury, Surender Rajasekaran, Jeremy W. Prokop +2 more

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Genetics in Medicine(2021)10.1038/s41436-021-01114-z

N/A

0DataRank · unranked

93 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +76 more