El Khattabi Laila - Institut Cochin, Université Paris Cité

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论文共 58 篇作者统计合作学者相似作者

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Stratification of the Risk of Ovarian Dysfunction by Studying the Complexity of Intermediate and Premutation Alleles of the FMR1 Gene

Juliette Quilichini,Sandrine Perol,Laurence Cuisset,Sarah Grotto,Corinne Fouveaut,Jean Claude Barbot,Camille Verebi,Penelope Jordan,Delphine Heron,Denise Molina-Gomes,Eva Pipiras,Michael Grynberg,Sophie Catteau-Jonard,Philippe Touraine,Sophie Christin-Maitre,Genevieve Plu-Bureau,Laila El Khattabi,Thierry Bienvenu

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 4 (2024)

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Usefulness of Early Morphological Ultrasound in Association with Cell-Free DNA Testing in Case of Atypical Serum Markers in First Trimester of Pregnancy: A Retrospective Study over 5 Years

Noemie Claudel,Olivia Anselem, Charlotte Buron-Fouque,Laila El Khattabi,Christelle Laguillier-Morizot,Penelope Jordan,Vassilis Tsatsaris,Jean Guibourdenche,Yoann Athiel

Journal of Gynecology Obstetrics and Human Reproductionno. 4 (2024): 102745

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Genetic Modifiers and Ascertainment Drive Variable Expressivity of Complex Disorders

Matthew Jensen,Corrine Smolen,Anastasia Tyryshkina,Lucilla Pizzo,Deepro Banerjee, Matthew Oetjens,Hermela Shimelis,Cora M Taylor,Vijay Kumar Pounraja,Hyebin Song,Laura Rohan,Emily Huber,Laila El Khattabi,Ingrid van de Laar,Rafik Tadros,Connie Bezzina,Marjon van Slegtenhorst,Janneke Kammeraad,Paolo Prontera,Jean-Hubert Caberg, Harry Fraser, Siddhartha Banka,Anke Van Dijck,Charles Schwartz,Els Voorhoeve,Patrick Callier,Anne-Laure Mosca-Boidron,Nathalie Marle,Mathilde Lefebvre,Kate Pope,Penny Snell,Amber Boys,Paul J Lockhart,Myla Ashfaq,Elizabeth McCready, Margaret Nowacyzk,Lucia Castiglia,Ornella Galesi,Emanuela Avola,Teresa Mattina,Marco Fichera, Maria Grazia Bruccheri,Giuseppa Maria Luana Mandarà,Francesca Mari,Flavia Privitera,Ilaria Longo,Aurora Curró,Alessandra Renieri,Boris Keren,Perrine Charles,Silvestre Cuinat,Mathilde Nizon,Olivier Pichon,Claire Bénéteau,Radka Stoeva,Dominique Martin-Coignard, Sophia Blesson,Cedric Le Caignec,Sandra Mercier,Marie Vincent,Christa Martin,Katrin Mannik,Alexandre Reymond,Laurence Faivre,Erik Sistermans,R Frank Kooy,David J Amor,Corrado Romano,Joris Andrieux,Santhosh Girirajan

medRxiv the preprint server for health sciences (2024)

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Chromatin Environment-Dependent Effects of DOT1L on Gene Expression in Male Germ Cells

Manon Coulee,Alberto de la Iglesia, Melina Blanco, Clara Gobe,Clementine Lapoujade, Come Ialy-Radio, Lucia Alvarez Gonzalez, Guillaume Meurice, Aurora Ruiz-Herrera,Pierre Fouchet,Julie Cocquet,Laila El Khattabi

crossref（2024）

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Performance of Cell-Free DNA Testing for Common Fetal Trisomies in Triplet Pregnancies

Hoda Zakaria,Pascale Kleinfinger,Laurence Lohmann,Jean-Marc Costa,Vassilis Tsatsaris,Laurent J. Salomon,Jean-Marie Jouannic,Jonathan Rosenblatt,Adele Demain,Alexandra Benachi,Laila El Khattabi,Alexandre J. Vivanti

PRENATAL DIAGNOSISno. 5 (2024): 555-561

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Prenatal Diagnosis of SLC25A24 Fontaine Progeroid Syndrome: Description of the Fetal Phenotype, Genotype and Detection of Parental Mosaicism

Emmanuelle Pannier, Abel Sekri,Nathalie Roux,Alexandre Vasiljevic,Laila El Khattabi,Nicolas Chatron,Sarah Grotto, Delphine Menzella,Gilles Grange, Florent Thebault,Jerome Massardier,Cecile Fourrage,Laurence Lohmann,Vassilis Tsatsaris,Audrey Putoux,Lucile Boutaud,Tania Attie-Bitach

BIRTH DEFECTS RESEARCHno. 7 (2024)

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MARK2 Variants Cause Autism Spectrum Disorder Via the Downregulation of WNT/β-catenin Signaling Pathway

Maolei Gong, Jiayi Li,Yijun Liu,Matheus Vernet Machado Bressan Wilke,Qian Li,Haoran Liu,Chen Liang,Joel A Morales-Rosado,Ana S.A. Cohen,Susan S. Hughes,Bonnie R. Sullivan, Valerie Waddell,Marie-José H. van den Boogaard,Richard H. van Jaarsveld,Ellen van Binsbergen,Koen L van Gassen,Tianyun Wang,Susan M. Hiatt,Michelle D. Amaral,Whitley V. Kelley,Jianbo Zhao,Weixing Feng,Changhong Ren,Yazhen Yu,Nicole J Boczek,Matthew J. Ferber,Carrie Lahner,Sherr Elliott,Yiyan Ruan,Mignot Cyril,Boris Keren,Hua Xie, Xiaoyan Wang,Bernt Popp,Christiane Zweier,Juliette Piard,Christine Coubes,Frederic Tran Mau-Them,Hana Safraou,Micheil Innes,Julie Gauthier,Jacques Michaud,Daniel C. Koboldt,Odent Sylvie,Marjolaine Willems,Wen-Hann Tan,Benjamin Cogne,Claudine Rieubland,Dominique Braun,Scott Douglas McLean,Konrad Platzer,Pia Zacher,Henry Oppermann,Lucie Evenepoel,Pierre Blanc,Laïla El Khattabi,Neshatul Haque,Nikita R. Dsouza,Michael T. Zimmermann,Raul Urrutia,Eric W Klee,Yiping Shen,Hongzhen Du,Zailong Qin,Chang-Mei Liu,Xiaoli Chen

The American Journal of Human Genetics (2024)

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Non-invasive Cell-Free DNA Prenatal Screening for Trisomy 21 As Part of Primary Screening Strategy in Twin Pregnancy

N. Claudel, M. Barrois,A. J. Vivanti,J. Rosenblatt,L. J. Salomon,J. -M. Jouannic,O. Picone,L. Carbillon,F. Vialard,E. Launay,V. Tsatsaris, E. Curis,L. El Khattabi

Ultrasound in obstetrics & gynecology (2023)

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Assortative Mating and Parental Genetic Relatedness Contribute to the Pathogenicity of Variably Expressive Variants

American journal of human geneticsno. 12 (2023): 2015-2028

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