Khalid Hussain

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 33

Top Venues

European journal of human genetics : EJHG

International journal of molecular sciences

The New England journal of medicine

Diabetes, metabolic syndrome and obesity : targets and therapy

Sidra Medical and Research Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Sidra Medical and Research Center Sep 01 2016

Qatar

Chief Endocrinology :: pediatrics

Publications

Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Hajar Dauleh, Rasha Amin, Maheen Pasha, Khalid Hussain
Adjuvant Alpelisib Therapy for Congenital Hyperinsulinism. The New England journal of medicine 390 (4) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Julia von Schnurbein, Stefanie Zorn, Adriana Nunziata, Stephanie Brandt, Barbara Moepps, Jan-Bernd Funcke, Khalid Hussain, I Sadaf Farooqi, Pamela Fischer-Posovszky, Martin Wabitsch
Classification of Congenital Leptin Deficiency. The Journal of clinical endocrinology and metabolism (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Hajar Dauleh, Rasha Amin, Maheen Pasha, Khalid Hussain
Adjuvant Alpelisib Therapy for Congenital Hyperinsulinism. The New England journal of medicine 390 (4) (2024)
Jan-Bernd Funcke, Barbara Moepps, Julian Roos, Julia von Schnurbein, Kenneth Verstraete, Elke Fröhlich-Reiterer, Katja Kohlsdorf, Adriana Nunziata, Stephanie Brandt, Alexandra Tsirigotaki, Ann Dansercoer, Elisabeth Suppan, Basma Haris, Klaus-Michael Debatin, Savvas N Savvides, I Sadaf Farooqi, Khalid Hussain, Peter Gierschik, Pamela Fischer-Posovszky, Martin Wabitsch
Rare Antagonistic Leptin Variants and Severe, Early-Onset Obesity. The New England journal of medicine 388 (24) (2023)
Idris Mohammed, Basma Haris, Tara Al-Barazenji, Dhanya Vasudeva, Sara Tomei, Iman Al Azwani, Hajar Dauleh, Saira Shehzad, Shiga Chirayath, Ghassan Mohamadsalih, Goran Petrovski, Amel Khalifa, Donald R Love, Mashael Al-Shafai, Khalid Hussain
Understanding the genetics of early onset obesity in a cohort of children from Qatar. The Journal of clinical endocrinology and metabolism (2023)
Idris Mohammed, Senthil Selvaraj, Wesam S Ahmed, Tara Al-Barazenji, Ayat S Hammad, Hajar Dauleh, Luís R Saraiva, Mashael Al-Shafai, Khalid Hussain
Functional Characterization of Novel MC4R Variants Identified in Two Unrelated Patients with Morbid Obesity in Qatar. International journal of molecular sciences 24 (22) (2023)
Huseyin Demirbilek, Dogus Vuralli, Basma Haris, Khalid Hussain
Managing Severe Hypoglycaemia in Patients with Diabetes: Current Challenges and Emerging Therapies. Diabetes, metabolic syndrome and obesity : targets and therapy 16 (2023)
Huseyin Demirbilek, Dogus Vuralli, Basma Haris, Khalid Hussain
Managing Severe Hypoglycaemia in Patients with Diabetes: Current Challenges and Emerging Therapies. Diabetes, metabolic syndrome and obesity : targets and therapy 16 (2023)
Iman Hawari, Johan Ericsson, Basirudeen Syed Ahamed Kabeer, Damien Chaussabel, Asma Alsulaiti, Sanaa A Sharari, Cristina Maccalli, Faiyaz Ahmad Khan, Khalid Hussain
Understanding the Mechanism of Diabetes Mellitus in a LRBA-Deficient Patient. Biology 11 (4) (2022)
Idris Mohammed, Basma Haris, Khalid Hussain
A Novel Homozygous MC2R Variant Leading to Type-1 Familial Glucocorticoid Deficiency. Journal of the Endocrine Society 6 (6) (2022)
Sanaa Sharari, Basirudeen Kabeer, Idris Mohammed, Basma Haris, Igor Pavlovski, Iman Hawari, Ajaz Ahmad Bhat, Mohammed Toufiq, Sara Tomei, Rebecca Mathew, Najeeb Syed, Sabah Nisar, Selma Maacha, Jean-Charles Grivel, Damien Chaussabel, Johan Ericsson, Khalid Hussain
Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi-Bickel Syndrome. Biomedicines 10 (9) (2022)
Basma Haris, Samuel Stafrace, Khalid Hussain
Type 2 Diabetes Mellitus in a 7 Year Old Girl. International medical case reports journal 15 (2022)
Basma Haris, Idris Mohammed, Sara Al-Khawaga, Khalid Hussain
Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family. International medical case reports journal 15 (2022)
Shayma M Ahmed, Basma Haris, Saras Saraswathi, Ahmed Elawwa, Amal Khalifa, Maryam AlMaadheed, Tasneem R Abdel-Karim, Noor Hamed, Houda Afyouni, Hajar Dauleh, Ahmed Shamekh, Mahmoud Al-Zyoud, Fawziya AlKhalaf, Goran Petrovski, Khalid Hussain
The epidemiology, clinical, biochemical, immunological and radiological features of youth onset type 2 diabetes mellitus in the state of Qatar. Diabetology international 13 (2) (2021)
Tasneem Abdel-Karim, Basma Haris, Houda Afyouni, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Zyoud, Ahmed Elawwa, Fawziya Al-Khalaf, Goran Petrovski, Khalid Hussain
The Epidemiology and Genetic Analysis of Children With Idiopathic Type 1 Diabetes in the State of Qatar. Journal of the Endocrine Society 5 (10) (2021)
Basma Haris, Idris Mohammed, Najeeb Syed, Khalid Fakhro, Khalid Hussain
Maturity-onset diabetes of the young (MODY) due to PDX1 mutation in a sib-pair diabetes family from Qatar. Clinical case reports 9 (12) (2021)
Sumaya Islam, Mehmet Tekman, Sarah E. Flanagan, Lisa Guay-Woodford, Khalid Hussain, Sian Ellard, Robert Kleta, Detlef Bockenhauer, Horia Stanescu, Daniela Iancu
Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD). Molecular genetics & genomic medicine (2021)
Basma Haris, Saras Saraswathi, Sara Al-Khawaga, Reem Hasnah, Amira Saeed, Shihab Mundekkadan, Noor Hamed, Houda Afyouni, Tasneem Abdel-Karim, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Al-Zyoud, Ahmed Shamekh, Ahmed Elawwa, Fawziya Al-Khalaf, Sabri Boughorbel, Goran Petrovski, Khalid Hussain
Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar. Journal of diabetes investigation (2021)
Basma Haris, Ahmed Abdellatief, Houda Afyouni, Tasneem Abdel-Karim, Shayma Mohammed, Amel Khalifa, Maryam Al-Maadheed, Mahmoud Zyoud, Ahmed Elawwa, Fawziya Al-Khalaf, Goran Petrovski, Khalid Hussain
The prevalence, immune profile, and clinical characteristics of children with celiac disease and type 1 diabetes mellitus in the state of Qatar. Journal of pediatric endocrinology & metabolism : JPEM 34 (11) (2021)
Parul Singh, Arun Rawat, Bara Al-Jarrah, Saras Saraswathi, Hoda Gad, Mamoun Elawad, Khalid Hussain, Mohammed A. Hendaus, Wesam Al-Masri, Rayaz Ahmed Malik, Souhaila Al Khodor, Anthony K Akobeng
Distinctive Microbial Signatures and Gut-Brain Crosstalk in Pediatric Patients with Coeliac Disease and Type 1 Diabetes Mellitus. International journal of molecular sciences 22 (4) (2021)
Idris Mohammed, Sara Al-Khawaga, David Bohanna, Abdusamea Shabani, Faiyaz Khan, Donald R Love, Zafar Nawaz, Khalid Hussain
Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype. Molecular genetics & genomic medicine 8 (6) (2020)
Basma Haris, Saras Saraswathi, Khalid Hussain
Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia. Therapeutic advances in endocrinology and metabolism 11 (2020)
Sanaa Sharari, Mohamad Abou-Alloul, Khalid Hussain, Faiyaz Ahmad
Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia. International journal of molecular sciences 21 (17) (2020)
Maha Sherif, Hüseyin Demirbilek, Atilla Çayır, Sophia Tahir, Busranur Erozan Cavdarli, Meliha Demiral, Ayse Nurcan Cebeci, Dogus Vuralli, Sofia Asim Rahman, Edip Unal, Gönül Büyükyılmaz, Rıza Taner Baran, Mehmet Nuri Özbek, Khalid Hussain
Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Meliha Demiral, Hüseyin Demirbilek, Kıymet Çelik, Nilufer Okur, Khalid Hussain, Mehmet Nuri Ozbek
Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life. Pediatric diabetes 21 (7) (2020)
Melissa Riachi, Firdevs Bas, Feyza Darendeliler, Khalid Hussain
A novel 3' untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus syndrome. Pediatric diabetes 20 (4) (2019)
Huseyin Demirbilek, Sonya Galcheva, Dogus Vuralli, Sara Al-Khawaga, Khalid Hussain
Ion Transporters, Channelopathies, and Glucose Disorders. International journal of molecular sciences 20 (10) (2019)
Emregül Işık, Hüseyin Demirbilek, Jayne A L Houghton, Sian Ellard, Sarah E. Flanagan, Khalid Hussain
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation Journal of clinical research in pediatric endocrinology 11 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Khalid Hussain