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Author/Creator Legius, Eric

1. Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies. Issue 8 (August 2017)

Authors:
Brison, Nathalie; van den Bogaert, Kris; Dehaspe, Luc; van den Oever, Jessica M. E.; Janssens, Katrien; Blaumeiser, Bettina; Peeters, Hilde; van Esch, Hilde; van Buggenhout, Griet; Vogels, Annick; de Ravel, Thomy; Legius, Eric; Devriendt, Koen; Vermeesch, Joris R.
Journal:
Obstetrical & gynecological survey
Issue:
Volume 72:Issue 8(2017)
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Record Type:
Journal Article
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2. Advancing RAS/RASopathy therapies: An NCI‐sponsored intramural and extramural collaboration for the study of RASopathies. Issue 4 (8th January 2020)

Authors:
Gross, Andrea M.; Frone, Megan; Gripp, Karen W.; Gelb, Bruce D.; Schoyer, Lisa; Schill, Lisa; Stronach, Beth; Biesecker, Leslie G.; Esposito, Dominic; Hernandez, Edjay Ralph; Legius, Eric; Loh, Mignon L.; Martin, Staci; Morrison, Deborah K.; Rauen, Katherine A.; Wolters, Pamela L.; Zand, Dina; Mc...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 4(2020)
Page Start:
866
Record Type:
Journal Article
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3. An incidental finding of maternal multiple myeloma by non invasive prenatal testing. (28th November 2017)

Authors:
Imbert‐Bouteille, Marion; Chiesa, Jean; Gaillard, Jean‐Baptiste; Dorvaux, Véronique; Altounian, Lucille; Gatinois, Vincent; Mousty, Eve; Finge, Sanae; Bourquard, Pascal; Vermeesch, Joris Robert; Legius, Eric; Vandenberghe, Peter
Journal:
Prenatal diagnosis
Issue:
Volume 37:Number 12(2017)
Page Start:
1257
Record Type:
Journal Article
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4. Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden. (20th August 2020)

Authors:
Morris, Stephanie M; Acosta, Maria T; Garg, Shruti; Green, Jonathan; Legius, Eric; North, Kathryn; Payne, Jonathan M; Weiss, Lauren A; Constantino, John N; Gutmann, David H
Journal:
Developmental medicine & child neurology
Issue:
Volume 63:Number 2(2021)
Page Start:
233
Record Type:
Journal Article
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6. Cancer Surveillance in Healthy Carriers of Germline Pathogenic Variants in BRCA1/2: A Review of Secondary Prevention Guidelines. (20th June 2020)

Authors:
Dullens, Boudewijn; de Putter, Robin; Lambertini, Matteo; Toss, Angela; Han, Sileny; Van Nieuwenhuysen, Els; Van Gorp, Toon; Vanderstichele, Adriaan; Van Ongeval, Chantal; Keupers, Machteld; Prevos, Renate; Celis, Valerie; Dekervel, Jeroen; Everaerts, Wouter; Wildiers, Hans; Nevelsteen, Ines; Nev...
Other Names:
Kleeff Jorg Academic Editor.
Journal:
Journal of oncology
Issue:
Volume 2020(2020)
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Journal Article
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7. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1. Issue 1 (26th October 2019)

Authors:
Koczkowska, Magdalena; Callens, Tom; Chen, Yunjia; Gomes, Alicia; Hicks, Alesha D.; Sharp, Angela; Johns, Eric; Uhas, Kim Armfield; Armstrong, Linlea; Bosanko, Katherine Armstrong; Babovic‐Vuksanovic, Dusica; Baker, Laura; Basel, Donald G.; Bengala, Mario; Bennett, James T.; Chambers, Chelsea; Cl...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
299
Record Type:
Journal Article
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8. Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85, 000 pregnancies. (May 2021)

Authors:
Lenaerts, Liesbeth; Brison, Nathalie; Maggen, Charlotte; Vancoillie, Leen; Che, Huiwen; Vandenberghe, Peter; Dierickx, Daan; Michaux, Lucienne; Dewaele, Barbara; Neven, Patrick; Floris, Giuseppe; Tousseyn, Thomas; Lannoo, Lore; Jatsenko, Tatjana; Bempt, Isabelle Vanden; Van Calsteren, Kristel; Va...
Journal:
EClinicalMedicine
Issue:
Volume 35(2021)
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Journal Article
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9. Comprehensive targeted next‐generation sequencing approach in the molecular diagnosis of gastrointestinal stromal tumor. Issue 4 (14th December 2020)

Authors:
Vanden Bempt, Isabelle; Vander Borght, Sara; Sciot, Raf; Spans, Lien; Claerhout, Sofie; Brems, Hilde; Lehnert, Stefan; Dehaspe, Luc; Fransis, Sabine; Neuville, Bart; Topal, Baki; Schöffski, Patrick; Legius, Eric; Debiec‐Rychter, Maria
Journal:
Genes, chromosomes & cancer
Issue:
Volume 60:Issue 4(2021)
Page Start:
239
Record Type:
Journal Article
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10. Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy. Issue 2 (10th November 2018)

Authors:
Suerink, Manon; Ripperger, Tim; Messiaen, Ludwine; Menko, Fred H; Bourdeaut, Franck; Colas, Chrystelle; Jongmans, Marjolijn; Goldberg, Yael; Nielsen, Maartje; Muleris, Martine; van Kouwen, Mariëtte; Slavc, Irene; Kratz, Christian; Vasen, Hans F; Brugiѐres, Laurence; Legius, Eric; Wimmer, Katharina
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 2(2019)
Page Start:
53
Record Type:
Journal Article
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