List of works - Sara S Kilic

A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets

scientific article

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

scientific article published on 22 June 2019

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

scientific article published on 14 May 2011

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

scientific article

Autoimmunity and hepatitis A vaccine in children

scientific article published on 01 January 2011

Central control of fever and female body temperature by RANKL/RANK

scientific article

Chronic Inflammatory Demyelinating Polyneuropathy in Common Variable Immunodeficiency ⬇️

scientific article published on 01 April 2012

Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation.

scientific article

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

scientific article

Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.

scientific article

Hematopoietic stem cell transplantation positively affects the natural history of cancer in Nijmegen breakage syndrome

scientific article published on 20 October 2020

Human CD3γ, but not CD3δ, haploinsufficiency differentially impairs γδ versus αβ surface TCR expression

scientific article

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

scientific article

Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations

scientific article

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

scientific article published on March 2015

Juvenile Idiopathic Inflammatory Myopathy in a Patient With Dyskeratosis Congenita Due to C16orf57 Mutation

scientific article published on 01 March 2016

Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions

scientific article

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

scientific article published on 07 July 2015

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

scientific article

Rituximab Therapy for Recalcitrant Idiopathic Sclerosing Orbital Inflammation

scientific article published on 08 October 2020

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

scientific article published on 19 September 2017

The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study

scientific article

The use of complementary and alternative medicine in patients with common variable immunodeficiency

scientific article published on January 1, 2011

Three different faces of TACI mutations

scientific article published on 11 March 2020

Transient hypogammaglobulinemia of infancy: clinical and immunologic features of 40 new cases

scientific article (publication date: December 2000)

ZNF341 controls STAT3 expression and thereby immunocompetence

scientific article published on 01 June 2018

List of works by Sara S Kilic

A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Autoimmunity and hepatitis A vaccine in children

Central control of fever and female body temperature by RANKL/RANK

Chronic Inflammatory Demyelinating Polyneuropathy in Common Variable Immunodeficiency ⬇️

Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation.

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.

Hematopoietic stem cell transplantation positively affects the natural history of cancer in Nijmegen breakage syndrome

Human CD3γ, but not CD3δ, haploinsufficiency differentially impairs γδ versus αβ surface TCR expression

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

Juvenile Idiopathic Inflammatory Myopathy in a Patient With Dyskeratosis Congenita Due to C16orf57 Mutation

Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

Rituximab Therapy for Recalcitrant Idiopathic Sclerosing Orbital Inflammation

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study

The use of complementary and alternative medicine in patients with common variable immunodeficiency

Three different faces of TACI mutations

Transient hypogammaglobulinemia of infancy: clinical and immunologic features of 40 new cases

ZNF341 controls STAT3 expression and thereby immunocompetence