Pegah Ghandil - Publications, H-index & Citations

Pegah Ghandil

institut national de la sante et de la recherche medicale (inserm)

14H指数

51论文数

2.6K被引数

收录论文 12

发表时间

Association of DRD2, DRD4 and COMT genes variants and their gene-gene interactions with antipsychotic treatment response in patients with schizophrenia

BMC PSYCHIATRY

IF3.6

2023-10-25

OAAI

Taheri, Narges; Pirboveiri, Rokhshid; Sayyah, Mehdi; Bijanzadeh, Mahdi; Ghandil, Pegah

The first report of two homozygous sequence variants inFKRPandSELENONgenes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes 伊朗与先天性肌营养不良综合征相关的两个纯合序列变异inFKRPandSELENONgenes的第一份报告: 临床表型的进一步扩展

JOURNAL OF GENE MEDICINE

IF2.2

2020-09-29

PREAI

Mohamadian, Malihe; Naseri, Mohsen; Ghandil, Pegah; Bahrami, Afsane; Momen, Ali Akbar

Effects of epigallocatechin gallate on total antioxidant capacity, biomarkers of systemic low-grade inflammation and metabolic risk factors in patients with type 2 diabetes mellitus: the role of FTO-rs9939609 polymorphism

ARCHIVES OF MEDICAL SCIENCE

IF3.3

2020-06-08

OAAI

Hosseini, Seyedahmad; Alipour, Meysam; Zakerkish, Mehrnoosh; Cheraghian, Bahman; Ghandil, Pegah

Association study between two polymorphisms of tumor necrosis factor ligand superfamily member 15 (TNFSF15) gene and ulcerative colitis in south-west of Iran

JOURNAL OF CELLULAR BIOCHEMISTRY

IF2.8

2018-12-16

PREAI

Taheri, Marzieh; Ghandil, Pegah; Hashemi, Seyyed Jalal; Ghafourian, Mehri; Zadeh, Abdol Rahim Masjedi; Ghadiri, Ata Allah

Mechanism of dysfunction of human variants of the IRAK4 kinase and a role for its kinase activity in interleukin-1 receptor signaling IRAK4激酶的人类变体功能障碍的机制及其激酶活性在interleukin-1受体信号传导中的作用

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2018-09-01

OAAI

De, Saurav; Karim, Fawziya; Kiessu, Ezechielle; Cushing, Leah; Lin, Lih-Ling; Ghandil, Pegah; Hoarau, Cyrille; Casanova, Jean-Laurent; Puel, Anne; Rao, Vikram R.

A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4

NATURE IMMUNOLOGY

IF27.6

2014-10-26

OAAI

Alsina, Laia; Israelsson, Elisabeth; Altman, Matthew C.; Dang, Kristen K.; Ghandil, Pegah; Israel, Laura; von Bernuth, Horst; Baldwin, Nicole; Qin, Huanying; Jin, Zongbo; Banchereau, Romain; Anguiano, Esperanza; Ionan, Alexei; Abel, Laurent; Puel, Anne; Picard, Capucine; Pascual, Virginia; Casanova, Jean Laurent; Chaussabel, Damien

Very Late-Onset Group B Streptococcus Meningitis, Sepsis, and Systemic Shigellosis due to Interleukin-1 Receptor-Associated Kinase-4 Deficiency

CLINICAL INFECTIOUS DISEASES

IF7.3

2009-11-01

OAAI

Krause, Jens C.; Ghandil, Pegah; Chrabieh, Maya; Casanova, Jean-Laurent; Picard, Capucine; Puel, Anne; Creech, C. Buddy

A polymorphism in the CCL2 chemokine gene is associated with asthma risk: a case-control and a family study in Tunisia

GENES AND IMMUNITY

IF4.5

2008-07-10

PREAI

Chelbi, H.; Ghadiri, A.; Lachheb, J.; Ghandil, P.; Hamzaoui, K.; Hamzaoui, A.; Combadiere, C.

Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

JOURNAL OF EXPERIMENTAL MEDICINE

IF10.6

2008-06-30

393

OAAI

de Beaucoudrey, Ludovic; Puel, Anne; Filipe-Santos, Orchidee; Cobat, Aurelie; Ghandil, Pegah; Chrabieh, Maya; Feinberg, Jacqueline; von Bernuth, Horst; Samarina, Arina; Janniere, Lucile; Fieschi, Claire; Stephan, Jean-Louis; Boileau, Catherine; Lyonnet, Stanislas; Jondeau, Guillaume; Cormier-Daire, Valerie; Le Merrer, Martine; Hoarau, Cyrille; Lebranchu, Yvon; Lortholary, Olivier; Chandesris, Marie-Olivia; Tron, Francois; Gambineri, Eleonora; Bianchi, Lucia; Rodriguez-Gallego, Carlos; Zitnik, Simona E.; Vasconcelos, Julia; Guedes, Margarida; Vitor, Artur Bonito; Marodi, Laszlo; Chapel, Helen; Reid, Brenda; Roifman, Chaim; Nadal, David; Reichenbach, Janine; Caragol, Isabel; Garty, Ben-Zion; Dogu, Figen; Camcioglu, Yildiz; Gulle, Sanyie; Sanal, Ozden; Fischer, Alain; Abel, Laurent; Stockinger, Birgitta; Picard, Capucine; Casanova, Jean-Laurent

PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits

DIABETES

IF7.5

2007-02-01

PREAI

Chelala, Claude; Duchatelet, Sabine; Joffret, Marie-Line; Bergholdt, Regine; Dubois-Laforgue, Daniele; Ghandil, Pegah; Pociot, Flemming; Caillat-Zucman, Sophie; Timsit, Jose; Julier, Cecile

Crohn's disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes

MOLECULAR GENETICS AND METABOLISM

IF3.5

2005-11-01

PREAI

Ghandil, P; Chelala, C; Dubois-Laforgue, D; Senée, V; Caillat-Zucman, S; Kockum, I; Luthman, H; Nerup, J; Pociot, F; Timsit, J; Julier, C

Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population

THROMBOSIS RESEARCH

IF3.4

2004-01-01

PREAI

Ghandil, P; Ghadiri, A; Farhud, D; Zeinali, S

研究方向