In memory of James F. Crow (1916–2012), a life dedicated to population genetics; with an updated list of his publications

por Otto, Paulo A.
Publicado 2012

Evolution of sex-ratio: Brief review with mathematical study of some simple novel models

por Otto, Paulo A.
Publicado 2021

Elementary Atlas of Drosophila melanogaster Mutations

por Otto, Paulo A.
Publicado 2022

A note on the population genetic consequences of delayed larval development in insects

por de Salles, Marcos Mattoso, Otto, Paulo A.
Publicado 2013

Penetrance rate estimation in autosomal dominant conditions

por Otto, Paulo A., Horimoto, Andréa R.V.R.
Publicado 2012

Haploid selection drives new gene male germline expression

por Raices, Julia B., Otto, Paulo A., Vibranovski, Maria D.
Publicado 2019

PENCALC: A program for penetrance estimation in autosomal dominant diseases

por Horimoto, Andréa R. V. Russo, Onodera, Márcio T., Otto, Paulo A.
Publicado 2010

A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome

por Alves, Leandro Ucela, Pardono, Eliete, Otto, Paulo A., Mingroni Netto, Regina Célia
Publicado 2015

Inbreeding levels in Northeast Brazil: Strategies for the prospecting of new genetic disorders

por Santos, Silvana, Kok, Fernando, Weller, Mathias, de Paiva, Francisco Rennan Lopes, Otto, Paulo A.
Publicado 2010

The clinical impact of chromosomal rearrangements with breakpoints upstream of the SOX9 gene: two novel de novo balanced translocations associated with acampomelic campomelic dyspl...

por Fonseca, Ana Carolina S, Bonaldi, Adriano, Bertola, Débora R, Kim, Chong A, Otto, Paulo A, Vianna-Morgante, Angela M
Publicado 2013

Men are the main COVID-19 transmitters: behavior or biology?

por Silva, Monize V. R., de Castro, Mateus V., Passos-Bueno, Maria Rita, Otto, Paulo A., Naslavsky, Michel S., Zatz, Mayana
Publicado 2022

Inbreeding estimates in human populations: Applying new approaches to an admixed Brazilian isolate

por Lemes, Renan B., Nunes, Kelly, Carnavalli, Juliana E. P., Kimura, Lilian, Mingroni-Netto, Regina C., Meyer, Diogo, Otto, Paulo A.
Publicado 2018

The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation

por Fonseca, Ana Carolina S., Bonaldi, Adriano, Fonseca, Simone A. S., Otto, Paulo A., Kok, Fernando, Bak, Mads, Tommerup, Niels, Vianna-Morgante, Angela M.
Publicado 2015

KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability

por Malvezzi, João VM, H Magalhaes, Ingrid, S Costa, Silvia, Otto, Paulo A, Rosenberg, Carla, Bertola, Debora R, LM Fernandes, Walter, Vianna-Morgante, Angela M, Krepischi, Ana CV
Publicado 2018

Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases

por Carneiro, Thaise NR, Krepischi, Ana CV, Costa, Silvia S, Tojal da Silva, Israel, Vianna-Morgante, Angela M, Valieris, Renan, Ezquina, Suzana AM, Bertola, Debora R, Otto, Paulo A, Rosenberg, Carla
Publicado 2018

The structure of first-cousin marriages in Brazil

por Otto, Paulo A., Lemes, Renan B., Farias, Allysson A., Weller, Mathias, Lima, Shirley O. A., Albino, Victor Alves, Marques-Alves, Yanna K., Pardono, Eliete, Bocangel, Magnolia A. P., Santos, Silvana
Publicado 2020