Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles von Nguyen, Ngoc Minh Phuong, Ge, Zhao-Jia, Reddy, Ramesh, Fahiminiya, Somayyeh, Sauthier, Philippe, Bagga, Rashmi, Sahin, Feride Iffet, Mahadevan, Sangeetha, Osmond, Matthew, Breguet, Magali, Rahimi, Kurosh, Lapensee, Louise, Hovanes, Karine, Srinivasan, Radhika, Van den Veyver, Ignatia B., Sahoo, Trilochan, Ao, Asangla, Majewski, Jacek, Taketo, Teruko, Slim, Rima

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The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients von Nguyen, Ngoc Minh Phuong, Khawajkie, Yassemine, Mechtouf, Nawel, Rezaei, Maryam, Breguet, Magali, Kurvinen, Elvira, Jagadeesh, Sujatha, Solmaz, Asli Ece, Aguinaga, Monica, Hemida, Reda, Harma, Mehmet Ibrahim, Rittore, Cécile, Rahimi, Kurosh, Arseneau, Jocelyne, Hovanes, Karine, Clisham, Ronald, Lenzi, Tiffanee, Scurry, Bonnie, Addor, Marie-Claude, Bagga, Rashmi, Nendaz, Genevieve Girardet, Finci, Vildana, Poke, Gemma, Grimes, Leslie, Gregersen, Nerine, York, Kayla, Bolze, Pierre-Adrien, Patel, Chirag, Mozdarani, Hossein, Puechberty, Jacques, Scotchie, Jessica, Fardaei, Majid, Harma, Muge, Gardner, R. J. McKinlay, Sahoo, Trilochan, Dudding-Byth, Tracy, Srinivasan, Radhika, Sauthier, Philippe, Slim, Rima

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Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes von Khawajkie, Yassemine, Mechtouf, Nawel, Nguyen, Ngoc Minh Phuong, Rahimi, Kurosh, Breguet, Magali, Arseneau, Jocelyne, Ronnett, Brigitte M., Hoffner, Lori, Lazure, Felicia, Arnaud, Marjolaine, Peers, Fabrice, Tan, Liane, Rafea, Basam Abu, Aguinaga, Monica, Horowitz, Neil S., Ao, Asangla, Tan, Seang Lin, Brown, Richard, Buckett, William, Surti, Urvashi, Hovanes, Karine, Sahoo, Trilochan, Sauthier, Philippe, Slim, Rima

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Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans von Djuric, Ugljesa, Bagga, Rashmi, Kircheisen, Renate, Rouleau, Guy A, Kuick, Rork, Ao, Asangla, Ratti, Bhawna, Murdoch, Sharlene, Slim, Rima, Mazhar, Batool, Seoud, Muheiddine, Khan, Rabia, Hanash, Samir

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Antagonism of EG-VEGF Receptors as Targeted Therapy for Choriocarcinoma Progression In Vitro and In Vivo von Traboulsi, Wael, Sergent, Frédéric, Boufettal, Houssine, Brouillet, Sophie, Slim, Rima, Hoffmann, Pascale, Benlahfid, Mohammed, Zhou, Qun Y, Balboni, Gianfranco, Onnis, Valentina, Bolze, Pierre A, Salomon, Aude, Sauthier, Philippe, Mallet, François, Aboussaouira, Touria, Feige, Jean J, Benharouga, Mohamed, Alfaidy, Nadia

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A novel NLRP7 protein-truncating mutation associated with discordant and divergent p57 immunostaining in diploid biparental and triploid digynic moles von Allias, Fabienne, Mechtouf, Nawel, Gaillot-Durand, Lucie, Hoffner, Lori, Hajri, Touria, Devouassoux-Shisheboran, Mojgan, Massardier, Jérôme, Golfier, François, Bolze, Pierre-Adrien, Surti, Urvashi, Slim, Rima

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Mono-pronuclear zygotes: a possible manifestation of androgenetic monospermic hydatidiform moles von Martin, Jacinta Hope, Slim, Rima

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The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread von Aguinaga, Mónica, Rezaei, Maryam, Monroy, Irma, Mechtouf, Nawel, Pérez, Javier, Moreno, Elsa, Valdespino, Yolotzin, Galaz, Carolina, Razo, Guadalupe, Medina, Daniela, Piña, Raúl, Slim, Rima

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A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage von Liang, Manqi, Suresh, Beena, Bareke, Eric, Choufani, Sanaa, Jagadeesh, Sujatha, Weksberg, Rosanna, Majewski, Jacek, Slim, Rima

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Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3 von Eisenberger, Tobias, Slim, Rima, Mansour, Ahmad, Nauck, Markus, Nürnberg, Gudrun, Nürnberg, Peter, Decker, Christian, Dafinger, Claudia, Ebermann, Inga, Bergmann, Carsten, Bolz, Hanno Jörn

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Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes von Khawajkie, Yassemine, Mechtouf, Nawel, Nguyen, Ngoc Minh Phuong, Rahimi, Kurosh, Breguet, Magali, Arseneau, Jocelyne, Ronnett, Brigitte M., Hoffner, Lori, Lazure, Felicia, Arnaud, Marjolaine, Peers, Fabrice, Tan, Liane, Rafea, Basam Abu, Aguinaga, Monica, Horowitz, Neil S., Ao, Asangla, Tan, Seang Lin, Brown, Richard, Buckett, William, Surti, Urvashi, Hovanes, Karine, Sahoo, Trilochan, Sauthier, Philippe, Slim, Rima

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Molecular genetics of the Usher syndrome in Lebanon: identification of 11 novel protein truncating mutations by whole exome sequencing von Reddy, Ramesh, Fahiminiya, Somayyeh, El Zir, Elie, Mansour, Ahmad, Megarbane, Andre, Majewski, Jacek, Slim, Rima

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NLRP7 Enhances Choriocarcinoma Cell Survival and Camouflage in an Inflammasome Independent Pathway von Reynaud, Déborah, Alfaidy, Nadia, Collet, Constance, Lemaitre, Nicolas, Sergent, Frederic, Miege, Céline, Soleilhac, Emmanuelle, Assi, Alaa Al, Murthi, Padma, Courtois, Gilles, Fauvarque, Marie-Odile, Slim, Rima, Benharouga, Mohamed, Abi Nahed, Roland

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Circulating Tumor DNA: A Potential Novel Diagnostic Approach in Gestational Trophoblastic Neoplasia von Bolze, Pierre-Adrien, Slim, Rima

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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C von Petit, Christine, Verpy, Elisabeth, Leibovici, Michel, Zwaenepoel, Ingrid, Liu, Xue-Zhong, Gal, Andreas, Salem, Nabiha, Mansour, Ahmad, Blanchard, Stéphane, Kobayashi, Ichiro, Keats, Bronya J.B, Slim, Rima

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NLRP7 and KHDC3L, the two maternal-effect proteins responsible for recurrent hydatidiform moles, co-localize to the oocyte cytoskeleton von Akoury, Elie, Zhang, Li, Ao, Asangla, Slim, Rima

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PLCZ1 Mutation and Failed IUI, ICSI, and Spontaneous Pregnancy Loss: Insights from a Case Study von Broojeni, Jalal Vallian, Safwat, Sylvia, Bareke, Eric, Majewski, Jacek, Abdalla, Ebtesam, Slim, Rima

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Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus von Slim, Rima, Fisher, Rosemary, Milhavet, Florian, Hemida, Reda, Rojas, Samantha, Rittore, Cécile, Bagga, Rashmi, Aguinaga, Monica, Touitou, Isabelle

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The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriages von Finley, Jenna, Hay, Sara, Oldzej, Jeannine, Meredith, Matthew M, Dzidic, Natasa, Slim, Rima, Aradhya, Swaroop, Hovanes, Karine, Sahoo, Trilochan

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Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles von Qian, JianHua, Nguyen, Ngoc Minh Phuong, Rezaei, Maryam, Huang, Bo, Tao, YongLing, Zhang, XiaoFei, Cheng, Qi, Yang, HanJin, Asangla, Ao, Majewski, Jacek, Slim, Rima

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