Hagit Baris Feldman

Also affiliated with Tel Aviv Sourasky Medical Center

Biochemistry, Genetics and Molecular BiologyMedicineImmunology and Microbiology

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

0.929Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817

Top 22%

0.929DataRank

Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

Papers

Driven by 26 papers — median percentile 78. Top paper: “Human genetic and immunological determinants of critical COVID-19 pneumonia”.

Human genetic and immunological determinants of critical COVID-19 pneumonia

Nature(2022)10.1038/s41586-022-04447-0

N/A

7.6DataRank · unranked

393 citations

Paul Bastard, COVID Human Genetic Effort, Adem Karbuz, Adrian Gervais, Ahmad Abou Tayoun +95 more

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

The Journal of Experimental Medicine(2022)10.1084/jem.20220131

N/A

2.0DataRank · unranked

117 citations

Daniela Matuozzo, Jérémie Le Pen, Danyel Lee, Leen Moens, Takaki Asano +94 more

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Genome Medicine(2023)10.1186/s13073-023-01173-8

N/A

1.5DataRank · unranked

78 citations

Estelle Talouarn, Astrid Marchal, Peng Zhang, Jérémy Manry, Yoann Seeleuthner +95 more

Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

The Journal of Experimental Medicine(2022)10.1084/jem.20220202

N/A

1.1DataRank · unranked

56 citations

Zhiyong Liu, Qian Zhang, Marcela Moncada‐Vélez, Laura Covill, Peng Zhang +94 more

Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study

The Lancet(2024)10.1016/s0140-6736(23)02358-9

N/A

0.995DataRank · unranked

28 citations

Voranush Chongsrisawat, Asena Pınar Sefer, Burcu Kolukısa, Jessica J. Jalbert, Karoline A. Meagher +35 more

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Clinical Genetics(2020)10.1111/cge.13817

Top 22%

0.929DataRank

Top 22%29 citations

Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov +45 more

A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

Cell(2020)10.1016/j.cell.2020.05.016

N/A

0.820DataRank · unranked

235 citations

Helen C. Su, Laurent Abel, Alessandro Aiuti, Saleh Al‐Muhsen, Andrés A. Arias +59 more

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Nature(2023)10.1038/s41586-023-06717-x

N/A

0.704DataRank · unranked

108 citations

Audrey V. Parent, Xian Liu, Axel Cederholm, Adrian Gervais, Jérémie Rosain +95 more

A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

Nature Immunology(2021)10.1038/s41590-021-01030-z

N/A

0.646DataRank · unranked

73 citations

Laurent Abel, Donald C. Vinh, Elżbieta Kaja, Beth A. Drolet, Qian Zhang +51 more

Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features

Science Advances(2021)10.1126/sciadv.abf2066

N/A

0.529DataRank · unranked

33 citations

Qin Wang, Naihua N. Gong, Alina Kurolap, Hagit Baris Feldman, Nikolas Boy +33 more

MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.001

N/A

0.406DataRank · unranked

14 citations

Maria Carla Borroto, Sadegheh Haghshenas, A Namasivayam, Jack Reilly, Michael A. Levy +61 more

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

medRxiv(2022)10.1101/2022.10.22.22281221

N/A

0.360DataRank · unranked

10 citations

Estelle Talouarn, Astrid Marchal, Jérémy Manry, Yoann Seeleuthner, Yu Zhang +95 more

Pozelimab for CHAPLE disease: results from in-trial interviews and clinical outcome assessments

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03277-9

N/A

0.326DataRank · unranked

5 citations

Ahmet Özen, Sarah Ollis, Hagit Baris Feldman, Andrew Yaworsky, Paolo Medrano +9 more

Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100300

N/A

0.306DataRank · unranked

6 citations

Elizabeth T. Cirulli, Iva Neveux, Evangelos Bellos, Ryan S. Thwaites, Kelly M. Schiabor Barrett +79 more

The seven enigmas of SARS-CoV-2: From the past to the future

Journal of Human Immunity(2025)10.70962/jhi.20250149

N/A

0.208DataRank · unranked

3 citations

Lisa M. Arkin, Paul Bastard, Alexandre Bolze, A. Borghesi, Petter Brodin +64 more

The patient experience of CHAPLE disease: results from interviews conducted as part of a clinical trial for an ultra-rare condition

Orphanet Journal of Rare Diseases(2025)10.1186/s13023-024-03436-y

N/A

0.179DataRank · unranked

2 citations

Ahmet Özen, Sarah Ollis, Hagit Baris Feldman, Andrew Yaworsky, Paolo Medrano +11 more

Autoantibodies against type I IFNs in patients with critical influenza pneumonia

The Journal of Experimental Medicine(2022)10.1084/jem.20220514

N/A

0DataRank · unranked

130 citations

Andrés Pizzorno, Lisa Miorin, Paul Bastard, Adrian Gervais, Tom Le Voyer +95 more

A founder variant in TBCB is associated with global developmental delay, autism spectrum, and spastic paraparesis

Genetics in Medicine(2025)10.1016/j.gim.2025.101569

N/A

0DataRank · unranked

0 citations

Chen Itzkovich, Alina Kurolap, Mordechai Shohat, Alexandra Dürr, Jean‐Madeleine de Sainte Agathe +15 more

Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.11.010

N/A

0DataRank · unranked

41 citations

Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Saleh Al‐Muhsen, Fahd Al‐Mulla +63 more

Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features

medRxiv(2020)10.1101/2020.10.26.20217109

N/A

0DataRank · unranked

0 citations

Qin Wang, Naihua N. Gong, Alina Kurolap, Hagit Baris Feldman, Nikolas Boy +33 more

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

The Journal of Experimental Medicine(2023)10.1084/jem.20220170

N/A

0DataRank · unranked

56 citations

Rebeca Pérez de Diego, Carlos Flores, Darawan Rinchai, Jordi Solé‐Violán, Àngela Deyà‐Martínez +92 more

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

Human Molecular Genetics(2020)10.1093/hmg/ddaa258

N/A

0DataRank · unranked

26 citations

Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen McInerney‐Leo, Paul Leo +29 more

A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

The Journal of Experimental Medicine(2024)10.1084/jem.20241413

N/A

0DataRank · unranked

13 citations

Jérémie Le Pen, Nicole A. de Weerd, Marcela Moncada‐Vélez, Marie Materna, Daniel Chieh-Ding Lin +89 more

Long-Read Structural and Epigenetic Profiling of a Kidney Tumor-Matched Sample with Nanopore Sequencing and Optical Genome Mapping

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.31.587463

N/A

0DataRank · unranked

1 citations

Zuzana Tulpová, Tahir Detinis Zur, Yael Michaeli, Jasline Deek, Gil Nifker +8 more

Long-read structural and epigenetic profiling of a kidney tumor-matched sample with nanopore sequencing and optical genome mapping

NAR Genomics and Bioinformatics(2025)10.1093/nargab/lqae190

N/A

0DataRank · unranked

7 citations

Zuzana Tulpová, Tahir Detinis Zur, Yael Michaeli, Jasline Deek, Gil Nifker +8 more

Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2

Nature Communications(2025)10.1038/s41467-025-65308-8

N/A

0DataRank · unranked

3 citations

Renée M. van der Sluis, Kennith Brian Castelino, Bao‐cun Zhang, Andreas Ronit, Thomas Zillinger +95 more

Hagit Baris Feldman

Indexed papers

Top data-sharing exemplar

Papers