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Louise Devisme

Developmental Mucin Gene Expression in the Human Respiratory Tract
1999 · Marie-Pierre Buisine, Louise Devisme, et al. · American Journal of Respiratory Cell and Molecular Biology · 199
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies
2012 · Louise Devisme, Céline Bouchet, et al. · Brain · 197
Mucin gene expression in human embryonic and fetal intestine
1998 · M P Buisine, L Devisme, et al. · Gut · 171
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Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway
2019 · Justyna A. Karolak, Marie Vincent, et al. · The American Journal of Human Genetics · 165
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Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly
2012 · Sandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, et al. · The American Journal of Human Genetics · 145
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Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases
2013 · Homa Adle-Biassette, Pascale Saugier-Veber, et al. · Acta Neuropathologica · 135
New insights into genotype–phenotype correlation for GLI3 mutations
2014 · Florence Démurger, Amale Ichkou, et al. · European Journal of Human Genetics · 130
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Developmental Mucin Gene Expression in the Gastroduodenal Tract and Accessory Digestive Glands. II. Duodenum and Liver, Gallbladder, and Pancreas
2000 · Marie-Pierre Buisine, Louise Devisme, et al. · Journal of Histochemistry & Cytochemistry · 117
Developmental Mucin Gene Expression in the Gastroduodenal Tract and Accessory Digestive Glands. I. Stomach: A Relationship to Gastric Carcinoma
2000 · Marie-Pierre Buisine, Louise Devisme, et al. · Journal of Histochemistry & Cytochemistry · 109
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation
2016 · Valentina Grampa, Marion Delous, et al. · PLoS Genetics · 103
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From normal respiratory mucosa to epidermoid carcinoma: Expression of human mucin genes
2000 · Marie-Christine Copin, Louise Devisme, et al. · International Journal of Cancer · 94
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C5orf42 is the major gene responsible for OFD syndrome type VI
2013 · Estelle Lopez, Christel Thauvin-Robinet, et al. · Human Genetics · 92
Radiographic features of osteogenesis imperfecta
2013 · Armelle Renaud, Julie Aucourt, et al. · Insights into Imaging · 90
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Immunolocalization of Inhibin and Activin α and βB Subunits and Expression of Corresponding Messenger RNAs in the Human Adult Testis
2003 · C. Marchetti, M. Hamdane, et al. · Biology of Reproduction · 87
Chronic histiocytic intervillositis of unknown etiology: Clinical features in a consecutive series of 69 cases
2010 · V. Marchaudon, L. Devisme, et al. · Placenta · 85
Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency
2005 · François Labarthe, Dries Dobbelaere, et al. · Journal of Hepatology · 84
SALL4 expression in gestational trophoblastic tumors: a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor
2016 · Morgane Stichelbout, Louise Devisme, et al. · Human Pathology · 69
Molecular heterogeneity in fetal forms of type II lissencephaly
2007 · C. Bouchet, M. Gonzales, et al. · Human Mutation · 64
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A case–control study of placental lesions associated with pre‐eclampsia
2012 · Louise Devisme, Benjamin Merlot, et al. · International Journal of Gynecology & Obstetrics · 61
Prenatal and early postnatal morphogenesis and growth of human laryngotracheal structures
2008 · Pierre Fayoux, Bruno Marciniak, et al. · Journal of Anatomy · 60
Expression of human mucin genes in normal kidney and renal cell carcinoma
2002 · X Leroy, M‐C Copin, et al. · Histopathology · 58
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Alveolar capillary dysplasia: a cause of persistent pulmonary hypertension of the newborn
2002 · Joumana Alameh, Ahmed Bachiri, et al. · European Journal of Pediatrics · 56
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew‐Wood syndrome): Report of eight cases including a living child and further evidence for autosomal recessive inheritance
2007 · David Chitayat, Hana Sroka, et al. · American Journal of Medical Genetics Part A · 55
Bardet‐Biedl syndrome: Antenatal presentation of forty‐five fetuses with biallelic pathogenic variants in known Bardet‐Biedl syndrome genes
2019 · Laura Mary, Kirsley Chennen, et al. · Clinical Genetics · 54
Determination of Endotracheal Tube Size in a Perinatal Population: An Anatomical and Experimental Study
2006 · Pierre Fayoux, Louise Devisme, et al. · Anesthesiology · 48
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Works count: 144
Citation count: 3,844
H-index: 34
I10-index: 74
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