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Genetics

D-Index
54
Citations
13554
World Ranking
3627
National Ranking
12

Overview

Carla Rosenberg is affiliated with the Universidade de São Paulo in Brazil and has a research focus predominantly within biochemistry, genetics, and molecular biology. Their scientific output includes a significant volume of publications, contributing extensively to the subfields of genetics, molecular biology, pediatrics, perinatology and child health, cancer research, and plant science.

Their research topics cover a range of genetic and genomic areas. Key topics include:

  • Genomic variations and chromosomal abnormalities
  • Genomics and rare diseases
  • Genetics and neurodevelopmental disorders
  • Congenital heart defects research
  • Prenatal screening and diagnostics
  • Chromosomal and genetic variations
  • Cancer genomics and diagnostics

Frequent publication venues for this researcher include:

  • Molecular Neurobiology
  • American Journal of Medical Genetics Part A
  • Clinical Genetics
  • Research Square
  • Annals of Human Genetics

Notable recent papers authored or co-authored by Carla Rosenberg are:

  • "Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome," 2021, The American Journal of Human Genetics
  • "Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder," 2020, Molecular Psychiatry
  • "DNA methylation as a key epigenetic player for hepatoblastoma characterization," 2021, Clinics and Research in Hepatology and Gastroenterology
  • "Understanding the Landscape of X-linked Variants Causing Intellectual Disability in Females Through Extreme X Chromosome Inactivation Skewing," 2020, Molecular Neurobiology
  • "Insights from the genetic characterization of central precocious puberty associated with multiple anomalies," 2020, Human Reproduction

Collaboration is an important aspect of their work, with frequent co-authors including Ana Cristina Victorino Krepischi, Silvia Souza da Costa, Débora Romeo Bertola, Laura Machado Lara Carvalho, and Angela Maria Vianna-Morgante. These partnerships reflect a network of expertise contributing to multidisciplinary studies within their field.

Best Publications

  • Consensus Statement : Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

    David T. Miller;Margaret P. Adam;Margaret P. Adam;Swaroop Aradhya;Leslie G. Biesecker

  • Mutations in the APC tumour suppressor gene cause chromosomal instability

    Riccardo Fodde;Jeroen Kuipers;Jeroen Kuipers;Carla Rosenberg;Ron Smits

  • TRPC1, a human homolog of a Drosophila store-operated channel

    Paul D. Wes;Jorge Chevesich;Andreas Jeromin;Carla Rosenberg

  • Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

    Charles Shaw-Smith;Alan M Pittman;Lionel Willatt;Howard Martin

  • Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

    Reinhard Ullmann;Gillian Turner;Maria Kirchhoff;Wei Chen

  • Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

    Carla Rosenberg;Carla Rosenberg;J. Knijnenburg;E. Bakker;A. M. Vianna-Morgante

  • Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

    D. A. Koolen;A. J. Sharp;A. J. Sharp;J. A. Hurst;H. V. Firth

  • Identification of genetic markers for prostatic cancer progression

    Janneke C Alers;Jenneke Rochat;Pieter-Jaap Krijtenburg;Wim C J Hop

  • Comparative Genomic Hybridization of Cancer of the Gastroesophageal Junction: Deletion of 14Q31–32.1 Discriminates between Esophageal (Barrett’s) and Gastric Cardia Adenocarcinomas

    Herman van Dekken;Eric Geelen;Winand N. M. Dinjens;B. P. L. Wijnhoven

  • Overrepresentation of the short arm of chromosome 12 is related to invasive growth of human testicular seminomas and nonseminomas.

    C Rosenberg;R J H L M Van Gurp;E Geelen;J W Oosterhuis

  • Genomic imbalances associated with müllerian aplasia

    Carola Cheroki;Ana C V Krepischi-Santos;Károly Szuhai;Volker Brenner

  • Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis.

    Judith V. M. G. Bovée;Anne-Marie Cleton-Jansen;Carla Rosenberg;Antonie H. M. Taminiau

  • Array-Based Comparative Genomic Hybridization Analysis Reveals Recurrent Chromosomal Alterations and Prognostic Parameters in Primary Cutaneous Large B-Cell Lymphoma

    Remco Dijkman;Cornelis P. Tensen;Ekaterina S. Jordanova;Jeroen Knijnenburg

  • Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair

    Marijke Bauters;Hilde Van Esch;Michael J. Friez;Odile Boespflug-Tanguy

  • Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

    J Dierlamm;C Rosenberg;M Stul;S Pittaluga

  • A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.

    Carola Jose Haven;Fung Ki Wong;Eveline W. C. M. van Dam;Rob van der Luijt

  • Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations

    A.C.V. Krepischi-Santos;A.M. Vianna-Morgante;F.S. Jehee;M.R. Passos-Bueno

  • Comparative genomic and in situ hybridization of germ cell tumors of the infantile testis

    Marijke Mostert;Carla Rosenberg;Hans Stoop;Monique Schuyer

  • Germline DNA copy number variation in familial and early-onset breast cancer

    Ana C.V. Krepischi;Ana C.V. Krepischi;Maria Isabel W. Achatz;Maria Isabel W. Achatz;Erika M.M. Santos;Silvia S. Costa

  • Genetic alterations on chromosome 16 and 17 are important features of ductal carcinoma in situ of the breast and are associated with histologic type.

    C. B. J. Vos;N. T. Ter Haar;C. Rosenberg;J. L. Peterse

Frequent Co-Authors

Dirce Maria Carraro
Dirce Maria Carraro AC Camargo Hospital
Karoly Szuhai
Karoly Szuhai Leiden University Medical Center
Hans J. Tanke
Hans J. Tanke Leiden University Medical Center
Anton K. Raap
Anton K. Raap Leiden University Medical Center
Maria Rita Passos-Bueno
Maria Rita Passos-Bueno Universidade de São Paulo
Lea T. Grinberg
Lea T. Grinberg University of California, San Francisco
Nigel P. Carter
Nigel P. Carter Wellcome Sanger Institute
Berenice B. Mendonca
Berenice B. Mendonca Universidade de São Paulo
Pancras C.W. Hogendoorn
Pancras C.W. Hogendoorn Leiden University Medical Center
Leendert H. J. Looijenga
Leendert H. J. Looijenga Princess Máxima Center

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