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Intestinal Metaplasia of the Esophagus in Children With Esophageal Atresia

Journal of pediatric gastroenterology and nutrition, 2017-07, Vol.65 (1), p.e1-e4

2017

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Multiple DICER1‐related tumors in a child with a large interstitial 14q32 deletion

Genes chromosomes & cancer, 2018-05, Vol.57 (5), p.223-230

2018

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Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1

Journal of medical genetics, 2022-07, Vol.59 (7), p.723-726

2022

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Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

Genetics in medicine, 2018-07, Vol.20 (7), p.745-753

2018

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Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome

Genes chromosomes & cancer, 2019-08, Vol.58 (8), p.602-604

2019

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A child with neuroblastoma and metachronous anaplastic sarcoma of the kidney: Underlying DICER1 syndrome?

Pediatric blood & cancer, 2020-12, Vol.67 (12), p.e28488-n/a

2020

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Association between proteinuria and placental pathology in preeclampsia: A retrospective study

SAGE open medicine, 2021-11, Vol.9, p.20503121211058053-20503121211058053

2021

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Risk Factors of Clinical Relapses in Pediatric Luminal Crohn's Disease: A Retrospective Cohort Study

The American journal of gastroenterology, 2022-04, Vol.117 (4), p.637-646

2022

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Germ-line and somatic DICER1 mutations in pineoblastoma

Acta neuropathologica, 2014-10, Vol.128 (4), p.583-595

2014

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Predictive biomarkers and initial analysis of maternal immune alterations in postpartum preeclampsia reveal an immune-driven pathology

Frontiers in immunology, 2024-04, Vol.15, p.1380629-1380629

2024

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Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome

Human pathology, 2015-06, Vol.46 (6), p.917-922

2015

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A case of neuroblastoma in DICER1 syndrome: Chance finding or noncanonical causation?

Pediatric blood & cancer, 2018-01, Vol.65 (1), p.n/a

2018

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Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome

American journal of medical genetics. Part A, 2020-04, Vol.182 (4), p.664-672

2020

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Germ-line and somatic DICER1 mutations in a pleuropulmonary blastoma

Pediatric blood & cancer, 2013-12, Vol.60 (12), p.2091-2092

2013

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A study of calretinin in Hirschsprung pathology, particularly in total colonic aganglionosis

Journal of pediatric surgery, 2013-05, Vol.48 (5), p.1037-1043

2013

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β Cell mass expansion during puberty involves serotonin signaling and determines glucose homeostasis in adulthood

JCI insight, 2022-11, Vol.7 (21)

2022

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54 FACTORS ASSOCIATED WITH TIME TO CLINICAL REMISSION IN PEDIATRIC LUMINAL CROHN'S DISEASE, A RETROSPECTIVE COHORT STUDY

Paediatrics & child health, 2022-10, Vol.27 (Supplement_3), p.e26-e26

2022

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55 RISK FACTORS ASSOCIATED WITH RELAPSES IN PEDIATRIC LUMINAL CROHN'S DISEASE, A RETROSPECTIVE COHORT STUDY

Paediatrics & child health, 2022-10, Vol.27 (Supplement_3), p.e26-e27

2022

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Endoscopic assessment of children with esophageal atresia: Lack of relationship of esophagitis and esophageal metaplasia to symptomatology

Canadian journal of gastroenterology, 2010-05, Vol.24 (5), p.312-316

2010

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Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers

JAMA network open, 2019-04, Vol.2 (4), p.e192906-e192906

2019

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Identification of divergent placental profiles in clinically distinct pregnancy complications revealed by the transcriptome

Placenta (Eastbourne), 2024-09, Vol.154, p.184-192

2024

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Distinct inflammatory profile in preeclampsia and postpartum preeclampsia reveal unique mechanisms

Biology of reproduction, 2019-01, Vol.100 (1), p.187-194

2019

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Interface hepatitis is associated with a high incidence of late graft fibrosis in a group of tightly monitored pediatric orthotopic liver transplantation patients

Liver transplantation, 2008-07, Vol.14 (7), p.946-955

2008

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In vivo dissection of the mouse tyrosine catabolic pathway with CRISPR-Cas9 identifies modifier genes affecting hereditary tyrosinemia type 1

Genetics (Austin), 2024-10, Vol.228 (2)

2024

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Intestinal Metaplasia of the Esophagus in Children With Esophageal Atresia

Multiple DICER1‐related tumors in a child with a large interstitial 14q32 deletion

Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome

A child with neuroblastoma and metachronous anaplastic sarcoma of the kidney: Underlying DICER1 syndrome?

Association between proteinuria and placental pathology in preeclampsia: A retrospective study

Risk Factors of Clinical Relapses in Pediatric Luminal Crohn's Disease: A Retrospective Cohort Study

Germ-line and somatic DICER1 mutations in pineoblastoma

Predictive biomarkers and initial analysis of maternal immune alterations in postpartum preeclampsia reveal an immune-driven pathology

Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome

A case of neuroblastoma in DICER1 syndrome: Chance finding or noncanonical causation?

Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome

Germ-line and somatic DICER1 mutations in a pleuropulmonary blastoma

A study of calretinin in Hirschsprung pathology, particularly in total colonic aganglionosis

β Cell mass expansion during puberty involves serotonin signaling and determines glucose homeostasis in adulthood

54 FACTORS ASSOCIATED WITH TIME TO CLINICAL REMISSION IN PEDIATRIC LUMINAL CROHN'S DISEASE, A RETROSPECTIVE COHORT STUDY

55 RISK FACTORS ASSOCIATED WITH RELAPSES IN PEDIATRIC LUMINAL CROHN'S DISEASE, A RETROSPECTIVE COHORT STUDY

Endoscopic assessment of children with esophageal atresia: Lack of relationship of esophagitis and esophageal metaplasia to symptomatology

Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers

Identification of divergent placental profiles in clinically distinct pregnancy complications revealed by the transcriptome

Distinct inflammatory profile in preeclampsia and postpartum preeclampsia reveal unique mechanisms

Interface hepatitis is associated with a high incidence of late graft fibrosis in a group of tightly monitored pediatric orthotopic liver transplantation patients

In vivo dissection of the mouse tyrosine catabolic pathway with CRISPR-Cas9 identifies modifier genes affecting hereditary tyrosinemia type 1

Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations

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