Classification algorithm for congenital Zika Syndrome: characterizations, diagnosis and validation von Veiga, Rafael V., Schuler-Faccini, Lavinia, França, Giovanny V. A., Andrade, Roberto F. S., Teixeira, Maria Glória, Costa, Larissa C., Paixão, Enny S., Costa, Maria da Conceição N., Barreto, Maurício L., Oliveira, Juliane F., Oliveira, Wanderson K., Cardim, Luciana L., Rodrigues, Moreno S.

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Thalidomide embryopathy: Follow-up of cases born between 1959 and 2010 von Kowalski, Thayne Woycinck, Sanseverino, Maria Teresa Vieira, Schuler-Faccini, Lavinia, Vianna, Fernanda Sales Luiz

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Microcephaly in Brazil: how to interpret reported numbers? von Victora, Cesar Gomes, Schuler-Faccini, Lavinia, Matijasevich, Alicia, Ribeiro, Erlane, Pessoa, André, Barros, Fernando Celso

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Congenital Zika virus syndrome in Brazil: a case series of the first 1501 livebirths with complete investigation von França, Giovanny V A, PhD, Schuler-Faccini, Lavinia, Prof, Oliveira, Wanderson K, MSc, Henriques, Claudio M P, MD, Carmo, Eduardo H, PhD, Pedi, Vaneide D, MSc, Nunes, Marília L, DVM, Castro, Marcia C, PhD, Serruya, Suzanne, PhD, Silveira, Mariângela F, MD, Barros, Fernando C, Prof, Victora, Cesar G, Prof

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Population medical genetics: translating science to the community von Giugliani, Roberto, Bender, Fernanda, Couto, Rowena, Bochernitsan, Aline, Brusius-Facchin, Ana Carolina, Burin, Maira, Amorim, Tatiana, Acosta, Angelina Xavier, Purificação, Antônio, Leistner-Segal, Sandra, Saraiva-Pereira, Maria Luiza, Jardim, Laura Bannach, Matte, Ursula, Riegel, Mariluce, Cardoso-Dos-Santos, Augusto César, Rodrigues, Graziella, Oliveira, Marcelo Zagonel de, Tagliani-Ribeiro, Alice, Heck, Selia, Dresch, Vanusa, Schuler-Faccini, Lavínia, Kubaski, Francyne

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Genotype‐phenotype correlations on epidermolysis bullosa with congenital absence of skin: A comprehensive review von Mariath, Luiza Monteavaro, Santin, Juliana Tosetto, Frantz, Jeanine Aparecida, Doriqui, Maria Juliana Rodovalho, Schuler‐Faccini, Lavínia, Kiszewski, Ana Elisa

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A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation von Adhikari, Kaustubh, Fuentes-Guajardo, Macarena, Quinto-Sánchez, Mirsha, Mendoza-Revilla, Javier, Camilo Chacón-Duque, Juan, Acuña-Alonzo, Victor, Jaramillo, Claudia, Arias, William, Lozano, Rodrigo Barquera, Pérez, Gastón Macín, Gómez-Valdés, Jorge, Villamil-Ramírez, Hugo, Hunemeier, Tábita, Ramallo, Virginia, Silva de Cerqueira, Caio C., Hurtado, Malena, Villegas, Valeria, Granja, Vanessa, Gallo, Carla, Poletti, Giovanni, Schuler-Faccini, Lavinia, Salzano, Francisco M., Bortolini, Maria- Cátira, Canizales-Quinteros, Samuel, Cheeseman, Michael, Rosique, Javier, Bedoya, Gabriel, Rothhammer, Francisco, Headon, Denis, González-José, Rolando, Balding, David, Ruiz-Linares, Andrés

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Inherited epidermolysis bullosa: update on the clinical and genetic aspects von Mariath, Luiza Monteavaro, Santin, Juliana Tosetto, Schuler-Faccini, Lavínia, Kiszewski, Ana Elisa

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Prevalence and antimicrobial resistance profile of Staphylococcus aureus in inherited epidermolysis bullosa: a cross‐sectional multicenter study in Brazil von Santin, Juliana T., Mariath, Luiza M., Rossato, Adriana M., Schuler‐Faccini, Lavínia, Kiszewski, Ana E.

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New cases of thalidomide embryopathy in Brazil von Schuler‐Faccini, Lavinia, Soares, Rosa Castalia Franca, de Sousa, Artur Custodio Moreira, Maximino, Claudia, Luna, Expedito, Schwartz, Ida Vanessa Doderlein, Waldman, Carolina, Castilla, Eduardo Enrique

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An overview of the genetic basis of epidermolysis bullosa in Brazil: discovery of novel and recurrent disease‐causing variants von Mariath, Luiza M., Santin, Juliana T., Frantz, Jeanine A., Doriqui, Maria J.R., Kiszewski, Ana E., Schuler‐Faccini, Lavínia

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Clusters of rare disorders and congenital anomalies in South America von Cardoso-Dos-Santos, Augusto César, Reales, Guillermo, Schuler-Faccini, Lavinia

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Clusters of oculocutaneous albinism in isolated populations in Brazil: A community genetics challenge von Moura, Paulyana, Cardoso-Dos-Santos, Augusto César, Schuler-Faccini, Lavinia

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Epidermolysis bullosa with congenital absence of skin: Clinical and genetic characterization of a 23‐case series von Mariath, Luiza M., Santin, Juliana T., Frantz, Jeanine A., Doriqui, Maria J.R., Schuler‐Faccini, Lavínia, Kiszewski, Ana E.

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A New Strategy for the Old Challenge of Thalidomide: Systems Biology Prioritization of Potential Immunomodulatory Drug (IMiD)-Targeted Transcription Factors von Kowalski, Thayne Woycinck, Feira, Mariléa Furtado, Lord, Vinícius Oliveira, Gomes, Julia do Amaral, Giudicelli, Giovanna Câmara, Fraga, Lucas Rosa, Sanseverino, Maria Teresa Vieira, Recamonde-Mendoza, Mariana, Schuler-Faccini, Lavinia, Vianna, Fernanda Sales Luiz

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The role of glial cells in Zika virus‐induced neurodegeneration von Quincozes‐Santos, André, Bobermin, Larissa Daniele, Costa, Naithan Ludian Fernandes, Thomaz, Natalie K., Almeida, Rômulo Rodrigo de Souza, Beys‐da‐Silva, Walter O., Santi, Lucélia, Rosa, Rafael L., Capra, Daniela, Coelho‐Aguiar, Juliana M., DosSantos, Marcos Fabio, Heringer, Manoela, Cirne‐Lima, Elizabeth O., Guimarães, Jorge Almeida, Schuler‐Faccini, Lavínia, Gonçalves, Carlos‐Alberto, Moura‐Neto, Vivaldo, Souza, Diogo Onofre

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Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015 von Schuler-Faccini, Lavinia, Ribeiro, Erlane M., Feitosa, Ian M.L., Horovitz, Dafne D.G., Cavalcanti, Denise P., Pessoa, André, Doriqui, Maria Juliana R., Neri, Joao Ivanildo, de Pina Neto, Joao Monteiro, Wanderley, Hector Y.C., Cernach, Mirlene, El-Husny, Antonette S., Pone, Marcos V.S., Serao, Cassio L.C., Sanseverino, Maria Teresa V.

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Fetal Alcohol Spectrum Disorders: Health Needs Assessment in Brazil von Rocha, Anastácia Guimarães, Souza, Paulo Ricardo Assis, Wachholz, Gabriela Elis, Fraga, Lucas Rosa, Sanseverino, Maria Teresa V., Terra, Anna Pires, Silva, André Anjos, Vianna, Fernanda Sales Luiz, Abeche, Alberto Mantovani, Larrandaburu, Mariela, Campo, Miguel, Schuler‐Faccini, Lavínia

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Editorial: Teratogenesis: Experimental Models, Mechanisms and Clinical Findings in Humans von Fraga, Lucas Rosa, Vianna, Fernanda Sales Luiz, Del Campo, Miguel, Sanseverino, Maria Teresa Vieira, Schuler-Faccini, Lavínia

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From bench to in silico and backwards: What have we done on genetics of recurrent pregnancy loss and implantation failure and where should we go next? von Gomes, Flavia Gobetti, Boquett, Juliano André, Kowalski, Thayne Woycinck, Bremm, João Matheus, Michels, Marcus Silva, Pretto, Luiza, Rockenbach, Marília Körbes, Vianna, Fernanda Sales Luiz, Schuler-Faccini, Lavinia, Sanseverino, Maria Teresa Vieira, Fraga, Lucas Rosa

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