M. Conley

M. Conley, L. Myers, D. Richter, 2001, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Hyper IgM Syndrome: a Report from the USIDNET Registry

R. Geha, C. Cunningham-Rundles, H. Ochs, 2016, Journal of Clinical Immunology.

Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

S. South, J. Casanova, W. Dolen, 2016, The New England journal of medicine.

Defects in early B‐cell development: comparing the consequences of abnormalities in pre‐BCR signaling in the human and the mouse

M. Conley, Y. Minegishi, J. Rohrer, 2000, Immunological reviews.

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies).

L. Notarangelo, M. Conley, Amos Etzioni, 1999, Clinical immunology.

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome.

A. Fischer, C. Cunningham-Rundles, A. Durandy, 2000, Clinical immunology.

Mutations of the human BTK gene coding for bruton tyrosine kinase in X‐linked agammaglobulinemia

M Vihinen, S P Kwan, M. Vihinen, 1999, Human mutation.

Mutations in btk in patients with presumed X-linked agammaglobulinemia.

M. Conley, Y. Minegishi, J. Rohrer, 1998, American journal of human genetics.

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling

A. Fischer, F. Deist, A. Smahi, 2001, Nature Genetics.

Genetic analysis of patients with defects in early B‐cell development

S. Shurtleff, H. Kanegane, T. Miyawaki, 2005, Immunological reviews.

Early defects in B cell development

M. Conley, 2002, Current opinion in allergy and clinical immunology.

Mutations in the Human λ5/14.1 Gene Result in B Cell Deficiency and Agammaglobulinemia

D. Campana, E. Coustan-Smith, M. Cooper, 1998, The Journal of experimental medicine.

Mutations in the mu heavy-chain gene in patients with agammaglobulinemia.

D. Campana, H. Trübel, E. Coustan-Smith, 1996, The New England journal of medicine.

Primary B cell immunodeficiencies: comparisons and contrasts.

D. Campana, E. Coustan-Smith, M. Conley, 2009, Annual review of immunology.

Immunodeficiencies: Comparisons and Contrasts

D. Campana, E. Coustan-Smith, M. Conley, 2009 .

Can Cancer Drugs Treat Immunodeficiency?

D. Fruman, M. Conley, 2013, Science.

Gene Conversion Events Contribute to the Polymorphic Variation of the Surrogate Light Chain Gene λ5/14.1

M. Conley, Y. Minegishi, J. Rohrer, 1999 .

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency.

J. Puck, M. Conley, P. Henthorn, 1997, Blood.

B-cell-specific demethylation of BTK, the defective gene in X-linked agammaglobulinemia

M. Conley, L. Shapiro, O. Parolini, 2004, Immunogenetics.

Direct quantitation of IgG subclasses 1, 2, and 3 bound to red cells by Rh1 (D) antibodies

M. Conley, A. Lobuglio, M. Khazaeli, 1988, Transfusion.

Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions.

M. Conley, Y. Minegishi, 2001, Immunity.

Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.

M. van der Burg, M. V. van Zelm, J. V. van Dongen, 2008, American journal of human genetics.

Severe combined immunodeficiency associated with nephrogenic diabetes insipidus and a deletion in the Xq28 region.

D. Bichet, M. Conley, M. Arthus, 2006, Clinical immunology.

Clinical findings leading to the diagnosis of X-linked agammaglobulinemia.

M. Conley, V. Howard, 2002, The Journal of pediatrics.

Discovery of single-gene inborn errors of immunity by next generation sequencing.

J. Casanova, M. Conley, 2014, Current opinion in immunology.

Agammaglobulinemia associated with BCR⁻ B cells and enhanced expression of CD19.

E. Coustan-Smith, M. Conley, A. K. Dobbs, 2011, Blood.

Effect of intravenous gammaglobulin (IVIG) on the platelet count in patients with Wiskott‐Aldrich syndrome

M. Conley, P. Mathew, 1995, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man.

R. Holcombe, A. Fauci, B. Taylor, 1987, Genomics.

A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features

Y. Crow, A. Gennery, J. Goodship, 2006, American journal of medical genetics. Part A.

Primary Antibody Deficiency Diseases

M. Conley, 2006 .

Genes required for B cell development.

M. Conley, 2003, The Journal of clinical investigation.

The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia

J. Belmont, M. Conley, O. Parolini, 1994, Immunogenetics.

Transcriptional Regulatory Elements Within the First Intron of Bruton's Tyrosine Kinase

M. Conley, J. Rohrer, 1998 .

X‐Linked Agammaglobulinemia: New Approaches to Old Questions based on the Identification of the Defective Gene

D. Campana, M. Conley, O. Parolini, 1994, Immunological reviews.

A chromosomal breakage syndrome with profound immunodeficiency.

W. W. Nichols, P. Nowell, N. Spinner, 1986, Blood.

Genetics of primary immunodeficiency diseases.

M. Conley, 2000, Reviews in immunogenetics.

Atypical Wiskott-Aldrich syndrome in a girl.

D. Campana, K. Siminovitch, M. Conley, 1992, Blood.

Atypical Wiskott-Aldrich syndrome in a girl

D. Campana, K. Siminovitch, M. Conley, 1992 .

Hyper IgM syndrome associated with defective CD40-mediated B cell activation.

D. Campana, E. Coustan-Smith, M. Conley, 1994, The Journal of clinical investigation.

Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire.

L. Staudt, A. Rosenwald, J. Casanova, 2004, Blood.

Primary immunodeficiencies: a rapidly evolving story.

J. Casanova, L. Notarangelo, M. Conley, 2013, The Journal of allergy and clinical immunology.

Molecular approaches to analysis of X-linked immunodeficiencies.

M. Conley, M. E. Conley, 1992, Annual review of immunology.

Expression of the gene defect in X-linked agammaglobulinemia.

J. Singer, M. Conley, W. Raskind, 1986, The New England journal of medicine.

Carrier detection in typical and atypical X-linked agammaglobulinemia.

J. Puck, M. Conley, 1988 .

Reconstitution of B cell function in murine models of immunodeficiency.

M. Conley, J. Rohrer, Andrea S. Porpiglia, 2003, Clinical immunology.

Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.

J. Puck, M. Conley, L. C. Bailey, 1993, American journal of human genetics.

Immunodeficiency disorders.

J. Puck, L. Lanier, M. Cooper, 2003, Hematology. American Society of Hematology. Education Program.

Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cells.

Toshiro K. Ohsumi, J. Orange, L. Notarangelo, 2014, The Journal of allergy and clinical immunology.

The spectrum of mutations in Btk that cause X-linked agammaglobulinemia.

M. Conley, J. Rohrer, 1995, Clinical immunology and immunopathology.

The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

J. Casanova, J. Franco, A. Bousfiha, 2015, Journal of Clinical Immunology.

A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside

J. Casanova, L. Notarangelo, R. Geha, 2013, Journal of Clinical Immunology.

Molecular basis of immunodeficiency

M. Conley, 2005 .

Clinical and molecular analysis of patients with defects in μ heavy chain gene

Mary Ellen Conley, Lennart Hammarström, C. Pignata, 2002 .

Analysis of SWAP-70 as a candidate gene for non-X-linked hyper IgM syndrome and common variable immunodeficiency.

C. Cunningham-Rundles, M. Conley, Y. Minegishi, 2001, Clinical immunology.

Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase.

J. Cleveland, M. Conley, O. Parolini, 1994, Human molecular genetics.

Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency.

J. Puck, A. Burks, M. Conley, 1991, The Journal of pediatrics.

A polymeric IgA response in serum can be produced by parenteral immunization.

M. Conley, J. Duchateau, D. Delacroix, 1987, Immunology.

In vitro regulation of IgA subclass synthesis. I. Discordance between plasma cell production and antibody secretion

M. Conley, W. Koopman, 1982, The Journal of experimental medicine.

Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulin.

D. Warnock, W. Cook, M. Conley, 2011, Journal of investigational allergology & clinical immunology.

Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts.

J. Orange, L. Notarangelo, C. Cunningham-Rundles, 2014, The Journal of allergy and clinical immunology.

Stem cell transplants for patients with X-linked agammaglobulinemia.

David A. Williams, J. Cunningham, M. Conley, 2003, Clinical immunology.

An Infant With Erythroderma, Skin Scaling, Chronic Emesis, and Intractable Diarrhea

E. Pivnick, M. Conley, D. B. Lew, 2009, Clinical pediatrics.

A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X‐linked gene WAS

T. Yang, M. Conley, A. K. Dobbs, 2007, Clinical genetics.

Lack of IgA in Cμ-deficient patients

L. Hammarström, M. Conley, J. Björkander, 2002, Nature Immunology.

Lack of IgA in C(mu)-deficient patients.

L. Hammarström, M. Conley, J. Björkander, 2002, Nature immunology.

Mutations in Igalpha (CD79a) result in a complete block in B-cell development.

D. Campana, F. Ersoy, E. Coustan-Smith, 1999, The Journal of clinical investigation.

Enteroviral Infection in a Patient with BLNK Adaptor Protein Deficiency

M. Conley, K. Warnatz, S. Unger, 2015, Journal of Clinical Immunology.

Successful Approach to Treatment of Helicobacter bilis Infection in X-Linked Agammaglobulinemia

L. Hoang, M. Conley, S. Turvey, 2012, Journal of Clinical Immunology.

Carrier detection in typical and X-linked agammaglobulinemia atypical

J. Puck, M. Conley, 1987 .

Successful treatment of neutropenia in the hyper-immunoglobulin M syndrome with granulocyte colony-stimulating factor.

M. Conley, J. Córdoba, W. Wang, 1994, The American journal of pediatric hematology/oncology.

Hypogammaglobulinemia and Reduced Numbers of B-Cells in Children With Myelodysplastic Syndrome

E. Coustan-Smith, M. Conley, Winfred C. Wang, 2001, Journal of pediatric hematology/oncology.

Quantitative effects of palivizumab and donor-derived T cells on chronic respiratory syncytial virus infection, lung disease, and fusion glycoprotein amino acid sequences in a patient before and after bone marrow transplantation.

J. Suzich, M. Conley, C. E. El Saleeby, 2004, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Multifocal adenocarcinoma of the stomach in a child with common variable immunodeficiency.

M. Conley, M. Ziegler, J. Boyle, 1988, Journal of pediatric gastroenterology and nutrition.

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. 1993.

T. Mohandas, J. Belmont, O. Witte, 2012, Journal of immunology.

Frequent mutations in SH2D1A (XLP) in males presenting with high‐grade mature B‐cell neoplasms

S. Shurtleff, M. Conley, E. Horwitz, 2013, Pediatric blood & cancer.

A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside

A. Fischer, J. Casanova, L. Notarangelo, 2013, Journal of Clinical Immunology.

Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1.

M. Conley, Y. Minegishi, J. Rohrer, 1999, Clinical immunology.

Diagnostic guidelines--An International Consensus document.

M. Conley, 1999, Clinical immunology.

Mutations in Ig α ( CD 79 a ) result in a complete block in B-cell development

D. Campana, F. Ersoy, E. Coustan-Smith, 2022 .

A chromosomal breakage syndrome with profound immunodeficiency

W. W. Nichols, P. Nowell, N. Spinner, 1986 .

A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.

J. Belmont, R. Gatti, M. Conley, 1996, The Journal of clinical investigation.

Serum levels of IgA1 and IgA2 in children and in patients with IgA deficiency.

M. Conley, S. Douglas, A. Arbeter, 1983, Molecular immunology.

Hypogammaglobulinemia: fifty years later.

M. Conley, 2002, Clinical immunology.

Novel mechanisms control the folding and assembly of lambda5/14.1 and VpreB to produce an intact surrogate light chain.

L. Hendershot, M. Conley, Y. Minegishi, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a pre-diversified immunoglobulin repertoire Running title: Circulating splenic marginal zone B cells in human

L. Staudt, A. Rosenwald, J. Casanova, 2004 .

Cow's milk allergy in a patient with hyper-IgE syndrome.

M. Conley, V. Hernandez-Trujillo, M. Jeng, 2004, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Cow's milk allergy in a patient with hyper-IgE

M. Conley, M. Jeng, D. B. Lew, 2004 .

Mutation Analysis of IL 2 RG in Human X-Linked Severe Combined Immunodeficiency

J. Puck, M. Conley, P. Henthorn, 1997 .

An essential role for the Zn2+ transporter ZIP7 in B cell development

J. Casanova, G. Rutter, M. van der Burg, 2019, Nature Immunology.

Are Patients with X-Linked Agammaglobulinemia at Increased Risk of Developing Acute Lymphoblastic Leukemia?

M. Conley, 2015, Journal of Clinical Immunology.

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

J. Casanova, L. Notarangelo, R. Geha, 2014, Front. Immunol..

Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

S. South, J. Casanova, W. Dolen, 2016, The New England journal of medicine.