D-Index & Metrics Best Publications

D-Index & Metrics

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 78 Citations 23,891 206 World Ranking 708 National Ranking 412
Medicine D-index 90 Citations 30,169 276 World Ranking 5890 National Ranking 3274

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Mutation
  • Internal medicine

Her main research concerns Immunology, Primary immunodeficiency, Severe combined immunodeficiency, Genetics and Autoimmune lymphoproliferative syndrome. Her Immunology study is mostly concerned with Job Syndrome, Immune system, Immunopathology, Lymphocyte and Immunodeficiency. Jennifer M. Puck interconnects Lymphocyte proliferation, Immunologic Deficiency Syndromes and Family medicine in the investigation of issues within Primary immunodeficiency.

Her Severe combined immunodeficiency research is multidisciplinary, relying on both Hematopoietic stem cell transplantation, Transplantation, Bone marrow and T-cell receptor excision circles. In Genetics, Jennifer M. Puck works on issues like Molecular biology, which are connected to Gene, Somatic cell, Mutant and CD3 Complex. The various areas that Jennifer M. Puck examines in her Autoimmune lymphoproliferative syndrome study include Fas ligand, Lymphoma and Lymphocyte homeostasis.

Her most cited work include:

  • Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome (1314 citations)
  • STAT3 Mutations in the Hyper-IgE Syndrome (894 citations)
  • Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 (681 citations)

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

Jennifer M. Puck mainly investigates Immunology, Severe combined immunodeficiency, Primary immunodeficiency, Genetics and Newborn screening. Her research integrates issues of Mutation and Autoimmune lymphoproliferative syndrome in her study of Immunology. Her work investigates the relationship between Autoimmune lymphoproliferative syndrome and topics such as Autoimmune disease that intersect with problems in Autoimmunity.

Her Severe combined immunodeficiency study incorporates themes from Hematopoietic stem cell transplantation, Transplantation, Genetic enhancement and T-cell receptor excision circles. Her Primary immunodeficiency research incorporates elements of Recombinant Human Hyaluronidase, Immunologic Deficiency Syndromes and Intensive care medicine. Within one scientific family, Jennifer M. Puck focuses on topics pertaining to Molecular biology under Genetics, and may sometimes address concerns connected to Mutant and Lymphocyte.

She most often published in these fields:

  • Immunology (51.59%)
  • Severe combined immunodeficiency (36.51%)
  • Primary immunodeficiency (16.14%)

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

  • Severe combined immunodeficiency (36.51%)
  • Immunology (51.59%)
  • Newborn screening (14.55%)

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

Jennifer M. Puck mainly investigates Severe combined immunodeficiency, Immunology, Newborn screening, Immune system and Transplantation. The concepts of her Severe combined immunodeficiency study are interwoven with issues in Hematopoietic stem cell transplantation, Busulfan, DCLRE1C, B cell and Genetic enhancement. She applies her multidisciplinary studies on Immunology and In patient in her research.

She works mostly in the field of Newborn screening, limiting it down to topics relating to Exome sequencing and, in certain cases, DNA sequencing. Her research in Transplantation intersects with topics in Hematopoietic cell, Omenn syndrome and Rituximab. Her Primary immunodeficiency study integrates concerns from other disciplines, such as Antibody and Intensive care medicine.

Between 2016 and 2021, her most popular works were:

  • International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity (421 citations)
  • The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies. (300 citations)
  • Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee (261 citations)

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

  • Gene
  • Mutation
  • Internal medicine

Her main research concerns Severe combined immunodeficiency, Transplantation, Newborn screening, Hematopoietic stem cell transplantation and Immunology. Her work deals with themes such as Immune system, Genetic enhancement and Pediatrics, which intersect with Severe combined immunodeficiency. Her study looks at the relationship between Newborn screening and fields such as T-cell receptor excision circles, as well as how they intersect with chemical problems.

Her Hematopoietic stem cell transplantation study combines topics from a wide range of disciplines, such as DCLRE1C and Oncology. Her Immunology research incorporates themes from Transplantation Conditioning and Busulfan. Her Primary immunodeficiency study combines topics in areas such as Immunologic Deficiency Syndromes and Family medicine.

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

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

Galen H Fisher;Fredric J Rosenberg;Stephen E Straus;Janet K Dale.
Cell (1995)

2123 Citations

STAT3 Mutations in the Hyper-IgE Syndrome

Steven M. Holland;Frank R. DeLeo;Houda Z. Elloumi;Amy P. Hsu.
The New England Journal of Medicine (2007)

1164 Citations

Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder

Bodo Grimbacher;Steven M. Holland;John I. Gallin;Frank Greenberg.
The New England Journal of Medicine (1999)

820 Citations

A prudent path forward for genomic engineering and germline gene modification

David Baltimore;Paul Berg;Michael Botchan;Dana Carroll.
Science (2015)

750 Citations

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

Hyung J. Chun;Lixin Zheng;Manzoor Ahmad;Jin Wang;Jin Wang.
Nature (2002)

750 Citations

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.

Rebecca H. Buckley;Richard I. Schiff;Sherrie E. Schiff;M.Louise Markert.
The Journal of Pediatrics (1997)

704 Citations

Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova.
Journal of Clinical Immunology (2015)

692 Citations

Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II

Jin Wang;Lixin Zheng;Adrian Lobito;Francis Ka Ming Chan.
Cell (1999)

687 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)

626 Citations

Primary immunodeficiencies: 2009 update

Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova.
The Journal of Allergy and Clinical Immunology (2009)

589 Citations

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