D-Index & Metrics Best Publications
Lennart Hammarström

Lennart Hammarström

Immunology
Sweden
2023

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Immunology D-index 89 Citations 28,174 397 World Ranking 687 National Ranking 10
Medicine D-index 89 Citations 28,678 419 World Ranking 8021 National Ranking 154

Research.com Recognitions

Awards & Achievements

2023 - Research.com Immunology in Sweden Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Antibody

His primary scientific interests are in Immunology, Genetics, Antibody, Common variable immunodeficiency and Selective IgA deficiency. Immunology is often connected to Genotype in his work. His Genetics research focuses on Gene, Allele, Mutation, Immunoglobulin class switching and Genetic linkage.

The Antibody study combines topics in areas such as Molecular biology, In vitro and Reoviridae. As a part of the same scientific study, Lennart Hammarström usually deals with the Common variable immunodeficiency, concentrating on MEDLINE and frequently concerns with Antibody deficiency, Clinical immunology and Differential diagnosis. The study incorporates disciplines such as IgA deficiency, Immunoglobulin A deficiency, Disease and Linkage disequilibrium in addition to Selective IgA deficiency.

His most cited work include:

  • The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases (1181 citations)
  • Helicobacter pylori SabA adhesin in persistent infection and chronic inflammation. (714 citations)
  • Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency (598 citations)

What are the main themes of his work throughout his whole career to date?

His scientific interests lie mostly in Immunology, Antibody, Genetics, Gene and Molecular biology. Immunology is a component of his Common variable immunodeficiency, Primary immunodeficiency, Immune system, Immunodeficiency and Selective IgA deficiency studies. His research integrates issues of Hypogammaglobulinemia and Autoimmunity in his study of Common variable immunodeficiency.

His studies deal with areas such as Severe combined immunodeficiency and Pediatrics, Newborn screening as well as Primary immunodeficiency. His biological study deals with issues like Microbiology, which deal with fields such as Lactobacillus. His Molecular biology study integrates concerns from other disciplines, such as Monoclonal antibody, Isotype, Subclass, B cell and Polyclonal antibodies.

He most often published in these fields:

  • Immunology (45.60%)
  • Antibody (36.57%)
  • Genetics (28.44%)

What were the highlights of his more recent work (between 2016-2021)?

  • Immunology (45.60%)
  • Primary immunodeficiency (15.35%)
  • Common variable immunodeficiency (13.32%)

In recent papers he was focusing on the following fields of study:

Lennart Hammarström mainly focuses on Immunology, Primary immunodeficiency, Common variable immunodeficiency, Immune system and Internal medicine. Single-nucleotide polymorphism is closely connected to Allele in his research, which is encompassed under the umbrella topic of Immunology. The concepts of his Primary immunodeficiency study are interwoven with issues in Severe combined immunodeficiency, Newborn screening, Cohort and Immunodeficiency.

His Common variable immunodeficiency research incorporates elements of Plasma cell, Haploinsufficiency, Gene and B-cell activating factor. The concepts of his Immune system study are interwoven with issues in Phenotype, Antibody and Pathogenesis. His work on Titer as part of general Antibody study is frequently connected to European union, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.

Between 2016 and 2021, his most popular works were:

  • Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing (86 citations)
  • Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency (86 citations)
  • Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant (70 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • DNA

Immunology, Primary immunodeficiency, Immunodeficiency, Internal medicine and Hypogammaglobulinemia are his primary areas of study. His study on Common variable immunodeficiency is often connected to Tyrosine kinase 2 as part of broader study in Immunology. Lennart Hammarström usually deals with Common variable immunodeficiency and limits it to topics linked to Autoimmunity and Phenotype.

His Primary immunodeficiency study combines topics from a wide range of disciplines, such as Immune dysregulation, Asymptomatic, Newborn screening and Cohort. His Immunodeficiency study incorporates themes from T cell and Disease. His Hypogammaglobulinemia study integrates concerns from other disciplines, such as Virology, Epstein–Barr virus, CD8 and NKG2D, Cytotoxic T cell.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

Vetrie D;Vorechovský I;Sideras P;Sideras P;Holland J.
Nature (1993)

1638 Citations

Helicobacter pylori SabA adhesin in persistent infection and chronic inflammation.

Jafar Mahdavi;Berit Sondén;Martina Hurtig;Farzad O. Olfat;Farzad O. Olfat.
Science (2002)

1043 Citations

Common variable immunodeficiency disorders: division into distinct clinical phenotypes

Helen Chapel;Mary Lucas;Martin Lee;Janne Bjorkander.
Blood (2008)

794 Citations

Clinical spectrum of X-linked hyper-IgM syndrome

Jacov Levy;Teresa Espanol-Boren;Carolin Thomas;Alain Fischer.
The Journal of Pediatrics (1997)

725 Citations

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

U Salzer;H M Chapel;A D B Webster;Q Pan-Hammarström.
Nature Genetics (2005)

717 Citations

Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel.
Frontiers in Immunology (2014)

660 Citations

International consensus document (icon): common variable immunodeficiency disorders

Francisco A. Bonilla;Isil Barlan;Helen Chapel;Beatriz Tavares Costa-Carvalho.
The Journal of Allergy and Clinical Immunology: In Practice (2016)

611 Citations

Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel.
The Journal of Allergy and Clinical Immunology (2007)

581 Citations

Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)

L Hammarström;I Vorechovsky;D Webster.
Clinical and Experimental Immunology (2000)

488 Citations

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

Gabriela Lopez-Herrera;Giacomo Tampella;Qiang Pan-Hammarström;Peer Herholz.
American Journal of Human Genetics (2012)

478 Citations

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