Richard J. Smith

NeuroscienceImmunology and MicrobiologyMedicine

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 36 papers. Top paper: “Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT‐RNR1 Genotype”.

Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT‐RNR1 Genotype

Clinical Pharmacology & Therapeutics(2021)10.1002/cpt.2309

N/A

0.705DataRank · unranked

109 citations

Joshua Wolf, Keito Hoshitsuki, Rachel Huddart, Kelly E. Caudle, Michelle Whirl‐Carrillo +7 more

CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

Frontiers in Genetics(2021)10.3389/fgene.2021.670727

N/A

0.524DataRank · unranked

32 citations

Matteo Breno, Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, Caterina Mele +8 more

Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum

Kidney International(2024)10.1016/j.kint.2024.09.012

N/A

0.477DataRank · unranked

23 citations

Gianluigi Ardissino, Vicky Brocklebank, Romy N. Bouwmeester, Arvind Bagga, Rob ter Heine +79 more

Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathy

Frontiers in Immunology(2025)10.3389/fimmu.2025.1589674

N/A

0.208DataRank · unranked

3 citations

Nicolò Ghiringhelli Borsa, Kai Wang, Amanda Taylor, Nicole C. Meyer, Michael B. Jones +11 more

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.29.222828

N/A

0DataRank · unranked

3 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +19 more

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Human Genetics(2021)10.1007/s00439-020-02254-z

N/A

0DataRank · unranked

28 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +21 more

Selective Binding of Heparin/Heparan Sulfate Oligosaccharides to Factor H and Factor H-Related Proteins: Therapeutic Potential for C3 Glomerulopathies

Frontiers in Immunology(2021)10.3389/fimmu.2021.676662

N/A

0DataRank · unranked

21 citations

Marissa L. Maciej-Hulme, Cansu Yanginlar, Melanie C. Hubers, Edwin Kellenbach, Mark de Graaf +6 more

TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62347

N/A

0DataRank · unranked

20 citations

Alejandro Ferrer, Carla Nishimura, Filippo Pinto e Vairo, Tristan Rey, Bruno Leheup +27 more

Monoclonal Gammopathy of Renal Significance Causes C3 Glomerulonephritis Via Monoclonal IgG Kappa Inhibition of Complement Factor H

Kidney International Reports(2021)10.1016/j.ekir.2021.06.015

N/A

0DataRank · unranked

11 citations

Sandra Carias Zuniga, Tejaswini Dhawale, Yuzhou Zhang, Richard J. Smith, Christopher D. Blosser +1 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w

N/A

0DataRank · unranked

17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Genetic testing hearing loss: The challenge of non syndromic mimics

International Journal of Pediatric Otorhinolaryngology(2021)10.1016/j.ijporl.2021.110872

N/A

0DataRank · unranked

17 citations

Natasha L. Rudy, Richard J. Smith, Nathaniel H. Robin, Catherine Gooch

Protein Structure Prediction Using a Maximum Likelihood Formulation of a Recurrent Geometric Network

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.03.458873

N/A

0DataRank · unranked

5 citations

Mallory R. Tollefson, Rose A. Gogal, Richard J. Smith, Mohammed AlQuraishi, Michael J. Schnieders +1 more

Alternative Complement Pathway Inhibition With Iptacopan for the Treatment of C3 Glomerulopathy-Study Design of the APPEAR-C3G Trial

Kidney International Reports(2022)10.1016/j.ekir.2022.07.004

N/A

0DataRank · unranked

77 citations

David Kavanagh, Marina Vivarelli, Matthias Meier, Yaqin Wang, Nicholas J.A. Webb +3 more

C3 glomerulopathy: Understanding an ultra‐rare complement‐mediated renal disease

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.31986

N/A

0DataRank · unranked

49 citations

Jill J. Hauer, Richard J. Smith, Amanda K. Heiderscheit

Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathy

Kidney International(2022)10.1016/j.kint.2022.05.027

N/A

0DataRank · unranked

41 citations

Jill J. Hauer, Florent Petitprez, Marion Rabant, Paula Vieira Martins, Véronique Baudouin +18 more

Protein therapeutics and their lessons: Expect the unexpected when inhibiting the multi‐protein cascade of the complement system

Immunological Reviews(2022)10.1111/imr.13164

N/A

0DataRank · unranked

25 citations

Richard J. Smith, Christoph Q. Schmidt

Complement Factor I Variants in Complement-Mediated Renal Diseases

Frontiers in Immunology(2022)10.3389/fimmu.2022.866330

N/A

0DataRank · unranked

17 citations

Renee X. Goodfellow, Nicolò Ghiringhelli Borsa, Hannah Dunlop, Stephen A. Presti, Nicole C. Meyer +8 more

The voltage-gated Ca2+ channel subunit α2δ-4 regulates locomotor behavior and sensorimotor gating in mice

PLoS ONE(2022)10.1371/journal.pone.0263197

N/A

0DataRank · unranked

12 citations

Ryotaro Omichi, Yoh-ichiro Iwasa, Richard J. Smith, Yuriy M. Usachev, Andrew F. Russo +3 more

Mutation-agnostic RNA interference with engineered replacement rescuesTmc1-related hearing loss

Life Science Alliance(2022)10.26508/lsa.202201592

N/A

0DataRank · unranked

13 citations

Miles J. Klimara, Hidekane Yoshimura, William D. Walls, Ryotaro Omichi, Cody West +4 more

Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy

Kidney International Reports(2023)10.1016/j.ekir.2023.11.025

N/A

0DataRank · unranked

22 citations

Yuzhou Zhang, Renee X. Goodfellow, Amanda Taylor, Nicole C. Meyer, Sarah M. Roberts +7 more

Iptacopan in Idiopathic Immune Complex–Mediated Membranoproliferative Glomerulonephritis: Protocol of the APPARENT Multicenter, Randomized Phase 3 Study

Kidney International Reports(2023)10.1016/j.ekir.2023.10.022

N/A

0DataRank · unranked

18 citations

Andrew S. Bomback, Matthias Meier, Yaqin Wang, Nicholas J.A. Webb, Uday Kiran Veldandi +3 more

Advances in cochlear gene therapies

Current Opinion in Pediatrics(2023)10.1097/mop.0000000000001273

N/A

0DataRank · unranked

14 citations

Richard J. Smith, Miles J. Klimara

Renin and renin blockade have no role in complement activity

Kidney International(2023)10.1016/j.kint.2023.11.005

N/A

0DataRank · unranked

11 citations

Bertha Martín, M. Ashley Spies, Sarah M. Roberts, Joel Nott, Renee X. Goodfellow +6 more

Modeling C3 glomerulopathies: C3 convertase regulation on an extracellular matrix surface

Frontiers in Immunology(2023)10.3389/fimmu.2022.1073802

N/A

0DataRank · unranked

3 citations

Nicole C. Meyer, Xue Xiao, Renee X. Goodfellow, Carla Nester, Yuzhou Zhang +2 more

Assessing Variants of Uncertain Significance Implicated in Hearing Loss Using a Comprehensive Deafness Proteome

Research Square(2023)10.21203/rs.3.rs-2508462/v1

N/A

0DataRank · unranked

2 citations

Rose A. Gogal, Amy Weaver, Amanda M. Schaefer, Robert J. Marini, Héla Azaiez +8 more

Functional evaluation of rare variants in complement factor I using a minigene assay

Frontiers in Immunology(2024)10.3389/fimmu.2024.1446081

N/A

0DataRank · unranked

5 citations

Nicolò Ghiringhelli Borsa, Amanda Taylor, Richard J. Smith, Yuzhou Zhang, Cobey J. H. Donelson

Prevalence of kidney health genetic variants in adults with sickle cell nephropathy

British Journal of Haematology(2024)10.1111/bjh.19525

N/A

0DataRank · unranked

1 citations

Xu Zhang, M. Adela Mansilla, Rima S. Zahr, Christie P. Thomas, Richard J. Smith +3 more

Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experiment

The Journal of Chemical Physics(2024)10.1063/5.0214652

N/A

0DataRank · unranked

1 citations

Aaron J. Nessler, Andrew Thiel, Hernan V. Bernabe, Rae Corrigan, Leah M. Cousineau +16 more

A predominately pulmonary activation of complement in a mouse model of severe COVID-19

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.31.596892

N/A

0DataRank · unranked

1 citations

Christine Wohlford-Lenane, Cobey J. Heinen, Shreya Ghimire, Biyun Xue, Timothy J. Boly +10 more

Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevance

Frontiers in Immunology(2025)10.3389/fimmu.2024.1527016

N/A

0DataRank · unranked

7 citations

Andrea Reparaz, Daniel L. Sanchez, Sheila Pinto, Lucia Juana Lopez, Héctor Martín Merinero +8 more

Complement is primarily activated in the lung in a mouse model of severe COVID-19

iScience(2025)10.1016/j.isci.2025.111930

N/A

0DataRank · unranked

6 citations

Christine Wohlford-Lenane, Cobey J. H. Donelson, Shreya Ghimire, Andrew L. Thurman, Biyun Xue +12 more

Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants

Scientific Reports(2020)10.1038/s41598-020-63256-5

N/A

0DataRank · unranked

87 citations

Lucía Borreguero, Kevin T. Booth, María Lachgar, P.L.M. Huygen, Manuela Villamar +11 more

Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlations

Human Genetics(2025)10.1007/s00439-025-02782-6

N/A

0DataRank · unranked

0 citations

William D. Walls, Kai Wang, Arthur Duston Odell, Diana L. Kolbe, Kevin T. Booth +3 more

Proteomic Analysis of Complement Proteins in Membranous Nephropathy

Kidney International Reports(2020)10.1016/j.ekir.2020.01.018

N/A

0DataRank · unranked

79 citations

Benjamin J. Madden, M. Cristine Charlesworth, Rishi Sharma, Amit Sethi, Hanna Dêbiec +6 more

Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome

Kidney International(2020)10.1016/j.kint.2020.05.028

N/A

0DataRank · unranked

15 citations

Robin Kremsdorf, C. John Sperati, Kammi Henriksen, Mari Mori, Renee X. Goodfellow +7 more

Hair Cell Transduction Efficiency of Single- and Dual-AAV Serotypes in Adult Murine Cochleae

Molecular Therapy — Methods & Clinical Development(2020)10.1016/j.omtm.2020.05.007

N/A

0DataRank · unranked

45 citations

Hidekane Yoshimura, Seiji B. Shibata, Luk H. Vandenberghe, Richard J. Smith, Ryotaro Omichi