Volume 142, Issue 5

Search all Human Genetics articles

May 2023

Special Issue on “The genetics of early-onset IBD”

Issue Editors:

Hagit Baris Feldman,
Alina Kurolap

8 articles in this issue

Special issue: the genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
Alina Kurolap
Hagit Baris Feldman
Editorial 27 April 2023 Pages: 595 - 597
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
Monogenic inflammatory bowel disease-genetic variants, functional mechanisms and personalised medicine in clinical practice
Aline Azabdaftari
Kelsey D. J. Jones
Holm H. Uhlig
Review 28 June 2022 Pages: 599 - 611
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
The genetics of monogenic intestinal epithelial disorders
Stephen J. Babcock
David Flores-Marin
Jay R. Thiagarajah
Review Open access 23 November 2022 Pages: 613 - 654
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
Beyond IBD: the genetics of other early-onset diarrhoeal disorders
Lorraine Stallard
Iram Siddiqui
Aleixo Muise
Review Open access 14 February 2023 Pages: 655 - 667
Part of 1 collection:

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
The genetics of non-monogenic IBD
Deborah Jans
Isabelle Cleynen
Review 31 January 2023 Pages: 669 - 682
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant
Alina Kurolap
David Hagin
Hagit Baris Feldman
Original Investigation 21 March 2022 Pages: 683 - 690
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy
Dina Marek-Yagel
Emily Stenke
Billy Bourke
Original Investigation Open access 09 September 2022 Pages: 691 - 696
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders
Phosphomannomutase 2 (PMM2) variants leading to hyperinsulinism-polycystic kidney disease are associated with early-onset inflammatory bowel disease and gastric antral foveolar hyperplasia
Fevronia Kiparissi
Antonia Dastamani
Kelsey D. J. Jones
Original Investigation Open access 11 February 2023 Pages: 697 - 704
Part of 2 collections:

The genetics of early onset IBD

The Genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders

Volume 142, Issue 5

Special issue: the genetics of early onset inflammatory bowel disease (IBD) and diarrheal disorders

Monogenic inflammatory bowel disease-genetic variants, functional mechanisms and personalised medicine in clinical practice

The genetics of monogenic intestinal epithelial disorders

Beyond IBD: the genetics of other early-onset diarrhoeal disorders

The genetics of non-monogenic IBD

CD55-deficiency in Jews of Bukharan descent is caused by the Cromer blood type Dr(a−) variant

Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy

Phosphomannomutase 2 (PMM2) variants leading to hyperinsulinism-polycystic kidney disease are associated with early-onset inflammatory bowel disease and gastric antral foveolar hyperplasia

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