H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Immunology D-index 63 Citations 15,091 145 World Ranking 1510 National Ranking 60

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Immune system
  • Cytokine

Cindy S. Ma mainly investigates Immunology, B cell, Cellular differentiation, Naive B cell and Immune system. Her is involved in several facets of Immunology study, as is seen by her studies on Interleukin 21, Immunoglobulin E, Autoimmunity, Antigen and Immunity. The various areas that Cindy S. Ma examines in her Interleukin 21 study include Interleukin 12 and CXCR5.

Her B cell research integrates issues from B-1 cell and Cell biology. Her Naive B cell study is focused on CD40 in general. Her Immune system course of study focuses on Cytokine and Signaling lymphocytic activation molecule.

Her most cited work include:

  • The transcriptional repressor Bcl-6 directs T follicular helper cell lineage commitment (870 citations)
  • Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3 (542 citations)
  • Circulating precursor CCR7(lo)PD-1(hi) CXCR5⁺ CD4⁺ T cells indicate Tfh cell activity and promote antibody responses upon antigen reexposure. (400 citations)

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

Her primary scientific interests are in Immunology, Immune system, Cell biology, B cell and Interleukin 21. As part of her studies on Immunology, she often connects relevant areas like CD40. Cindy S. Ma has researched Cell biology in several fields, including Cellular differentiation, Cytokine, B-1 cell, Mutation and Receptor.

She usually deals with Cellular differentiation and limits it to topics linked to CXCR5 and BCL6. Her work in B cell addresses issues such as Molecular biology, which are connected to fields such as Transcription factor. The various areas that Cindy S. Ma examines in her Interleukin 21 study include Natural killer T cell, Interleukin 12 and IL-2 receptor.

She most often published in these fields:

  • Immunology (105.88%)
  • Immune system (42.25%)
  • Cell biology (42.25%)

What were the highlights of her more recent work (between 2018-2021)?

  • Immunology (105.88%)
  • Immune system (42.25%)
  • CD8 (19.25%)

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

Cindy S. Ma focuses on Immunology, Immune system, CD8, Immunodeficiency and Immunity. The concepts of her Immunology study are interwoven with issues in Dominant-Negative Mutation, Disease and Gene isoform. Her Immune system study integrates concerns from other disciplines, such as Hematopoietic stem cell transplantation, Germinal center and Lymphocyte.

Her research on Germinal center also deals with topics like

  • Cell biology most often made with reference to Immunopathology,
  • FOXP3 which intersects with area such as Cancer research. The study incorporates disciplines such as Mycobacterial disease, Transcription factor, Cytoskeleton, Actin and Primary immunodeficiency in addition to Immunity. Her research integrates issues of Humoral immunity, Cellular differentiation and Atopic dermatitis in her study of Cytokine.

Between 2018 and 2021, her most popular works were:

  • An essential role for the Zn2+ transporter ZIP7 in B cell development (31 citations)
  • An essential role for the Zn2+ transporter ZIP7 in B cell development (31 citations)
  • Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome. (23 citations)

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

  • Gene
  • Immune system
  • Cytokine

Her primary scientific interests are in Immunity, Cytokine, Cell biology, Germinal center and Immune system. Her work deals with themes such as Primary immunodeficiency, Actin cytoskeleton, Cytoskeleton and Actin, which intersect with Immunity. In her study, which falls under the umbrella issue of Cytokine, Cancer research is strongly linked to Plasma cell.

Her Cancer research research is multidisciplinary, incorporating perspectives in Connective Tissue Disorder, Haploinsufficiency, Signal transduction, Extracellular matrix and Chronic mucocutaneous candidiasis. She interconnects Humoral immunity, Cell and Immunopathology in the investigation of issues within Cell biology. Her studies deal with areas such as Immune dysregulation and Interleukin 21 as well as Germinal center.

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 transcriptional repressor Bcl-6 directs T follicular helper cell lineage commitment

Di Yu;Sudha Rao;Louis M Tsai;Sau K Lee.
Immunity (2009)

1140 Citations

Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3

Cindy S. Ma;Gary Y.J. Chew;Nicholas Simpson;Archana Priyadarshi.
Journal of Experimental Medicine (2008)

663 Citations

The origins, function, and regulation of T follicular helper cells.

Cindy S. Ma;Elissa K. Deenick;Elissa K. Deenick;Marcel Batten;Marcel Batten;Stuart G. Tangye;Stuart G. Tangye.
Journal of Experimental Medicine (2012)

534 Citations

Cytokine-Mediated Regulation of Human B Cell Differentiation into Ig-Secreting Cells: Predominant Role of IL-21 Produced by CXCR5+ T Follicular Helper Cells

Vanessa L. Bryant;Vanessa L. Bryant;Vanessa L. Bryant;Cindy S. Ma;Cindy S. Ma;Danielle T. Avery;Danielle T. Avery;Ying Li.
Journal of Immunology (2007)

483 Citations

The good, the bad and the ugly - TFH cells in human health and disease.

Stuart G. Tangye;Stuart G. Tangye;Cindy S. Ma;Cindy S. Ma;Robert Brink;Robert Brink;Elissa K. Deenick;Elissa K. Deenick.
Nature Reviews Immunology (2013)

458 Citations

Circulating precursor CCR7(lo)PD-1(hi) CXCR5⁺ CD4⁺ T cells indicate Tfh cell activity and promote antibody responses upon antigen reexposure.

Jing He;Louis M Tsai;Yew A Leong;Xin Jack Hu;Xin Jack Hu.
Immunity (2013)

423 Citations

Regulation of NKT cell development by SAP, the protein defective in XLP.

Kim E. Nichols;Kim E. Nichols;Jamie Hom;Shun You Gong;Arupa Ganguly.
Nature Medicine (2005)

416 Citations

B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

Danielle T. Avery;Elissa K. Deenick;Elissa K. Deenick;Cindy S. Ma;Cindy S. Ma;Santi Suryani;Santi Suryani.
Journal of Experimental Medicine (2010)

331 Citations

Early commitment of naïve human CD4(+) T cells to the T follicular helper (T(FH)) cell lineage is induced by IL-12.

Cindy S Ma;Santi Suryani;Santi Suryani;Danielle T Avery;Anna Chan.
Immunology and Cell Biology (2009)

326 Citations

Regulation of Cellular and Humoral Immune Responses by the SLAM and SAP Families of Molecules

Cindy S. Ma;Kim E. Nichols;Stuart G. Tangye.
Annual Review of Immunology (2007)

301 Citations

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