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Author/Creator Messiaen, Ludwine M.

1. Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African‐American brothers. Issue 8 (4th July 2013)

Authors:
Balikcioglu, Pinar Gumus; Gómez, Ricardo; Vargas, Alfonso; Aradhya, Swaroop; Messiaen, Ludwine M.; Lacassie, Yves
Journal:
American journal of medical genetics
Issue:
Volume 161:Issue 8(2013:Aug.)
Page Start:
2105
Record Type:
Journal Article
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2. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Issue 3 (14th November 2016)

Authors:
Sites, Emily R.; Smolarek, Teresa A.; Martin, Lisa J.; Viskochil, David H.; Stevenson, David A.; Ullrich, Nicole J.; Messiaen, Ludwine M.; Schorry, Elizabeth K.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 3(2017)
Page Start:
647
Record Type:
Journal Article
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3. Breast cancer risk and germline genomic profiling of women with neurofibromatosis type 1 who developed breast cancer. Issue 1 (30th September 2017)

Authors:
Wang, Xia; Teer, Jamie K.; Tousignant, Renee N.; Levin, Albert M.; Boulware, David; Chitale, Dhananjay A.; Shaw, Brandon M.; Chen, Zhihua; Zhang, Yonghong; Blakeley, Jaishri O.; Acosta, Maria T.; Messiaen, Ludwine M.; Korf, Bruce R.; Tainsky, Michael A.
Journal:
Genes, chromosomes & cancer
Issue:
Volume 57:Issue 1(2018)
Page Start:
19
Record Type:
Journal Article
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4. 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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5. From process to progress—2017 International Conference on Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis. Issue 6 (25th March 2019)

Authors:
Ferner, Rosalie E.; Bakker, Annette; Elgersma, Ype; Evans, D. Gareth R.; Giovannini, Marco; Legius, Eric; Lloyd, Alison; Messiaen, Ludwine M.; Plotkin, Scott; Reilly, Karlyne M.; Schindeler, Aaron; Smith, Miriam J.; Ullrich, Nicole J.; Widemann, Brigitte; Sherman, Larry S.
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 6(2019)
Page Start:
1098
Record Type:
Journal Article
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8. Targeted massively parallel sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas: An analysis of 51 individuals in a single‐center experience. Issue 1 (15th November 2021)

Authors:
Piotrowski, Arkadiusz; Koczkowska, Magdalena; Poplawski, Andrzej B.; Bartoszewski, Rafał; Króliczewski, Jarosław; Mieczkowska, Alina; Gomes, Alicia; Crowley, Michael R.; Crossman, David K.; Chen, Yunjia; Lao, Ping; Serra, Eduard; Llach, Meritxell C.; Castellanos, Elisabeth; Messiaen, Ludwine M.
Journal:
Human mutation
Issue:
Volume 43:Issue 1(2022)
Page Start:
74
Record Type:
Journal Article
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