Ganka Douglas

1.6k total citations
13 papers, 336 citations indexed

About

Ganka Douglas is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ganka Douglas has authored 13 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ganka Douglas's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (3 papers). Ganka Douglas is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (3 papers). Ganka Douglas collaborates with scholars based in United States, Netherlands and Switzerland. Ganka Douglas's co-authors include Marwan Shinawi, Megan T. Cho, Daniel J. Parente, Berivan Baskin, Gabriel C. Araujo, Eric Schmitt, Kyle Retterer, Bekim Sadiković, William J. Craigen and Megan Landsverk and has published in prestigious journals such as PLoS ONE, Bone and Human Mutation.

In The Last Decade

Ganka Douglas

13 papers receiving 316 citations

Peers

Countries citing papers authored by Ganka Douglas

Since Specialization

Citations

This map shows the geographic impact of Ganka Douglas's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ganka Douglas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ganka Douglas more than expected).

Fields of papers citing papers by Ganka Douglas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ganka Douglas. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ganka Douglas. The network helps show where Ganka Douglas may publish in the future.

Co-authorship network of co-authors of Ganka Douglas

This figure shows the co-authorship network connecting the top 25 collaborators of Ganka Douglas. A scholar is included among the top collaborators of Ganka Douglas based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ganka Douglas. Ganka Douglas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Uniparental disomy in a population of 32,067 clinical exome trios 2021 ·Genetics in Medicine ·Julie Scuffins, Jennifer Keller‐Ramey, (unknown), Ganka Douglas, Rebecca I. Torene, Vladimir G. Gainullin, Jane Juusola, Jeanne Meck, Kyle Retterer	38
2	Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability 2019 ·Clinical Genetics ·Alban Ziegler, Patricia I. Bader, Kirsty McWalter, Ganka Douglas, (unknown), Céline Bris, Stéphanie Rouleau, R. Coutant, Estelle Colin, Dominique Bonneau	8
3	Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants 2018 ·Human Mutation ·Jorge L. Granadillo, Wendy K. Chung, Leah Hecht, Nicole Corsten‐Janssen, Daniel Wegner, (unknown), Tomi L. Toler, Daniel Pineda‐Alvarez, Ganka Douglas, Joshua Murphy, Joshua S. Shimony, Marwan Shinawi	26
4	Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes 2018 ·Bone ·(unknown), Ebtesam Abdalla, Andrea Superti‐Furga, William H. McAlister, Lisa E. Kratz, Sheila Unger, Béryl Royer‐Bertrand, Belinda Campos‐Xavier, (unknown), (unknown), (unknown), David B. Wilson, Ganka Douglas, Beth A. Kozel, Marwan Shinawi	8
5	De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features 2018 ·American Journal of Medical Genetics Part A ·Ganka Douglas, Megan T. Cho, Aida Telegrafi, Susan Winter, Jason Carmichael, Elaine H. Zackai, Matthew A. Deardorff, Margaret Harr, Linford Williams, (unknown), Angelika Erwin, Theresa A. Grebe, Kyle Retterer, Jane Juusola	23
6	Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity 2016 ·American Journal of Medical Genetics Part A ·Daniel J. Parente, (unknown), Berivan Baskin, Ganka Douglas, Megan T. Cho, Gabriel C. Araujo, Marwan Shinawi	79
7	De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features 2015 ·Molecular Case Studies ·Akemi Tanaka, Megan T. Cho, Kyle Retterer, Julie R. Jones, C. Nowak, Jessica Douglas, Yong‐hui Jiang, Allyn McConkie‐Rosell, G. Bradley Schaefer, Julie Kaylor, (unknown), Aida Telegrafi, Bethany Friedman, Ganka Douglas, Kristin G. Monaghan, Wendy K. Chung	25
8	Characterization of a recurrent 3.8kb deletion involving exons 17a and 17b within the CFTR gene 2012 ·Journal of Cystic Fibrosis ·Sha Tang, (unknown), Blair Stevens, Ganka Douglas, Sally Mason, Eric Schmitt, Christine M. Eng, Marcia Katz, Ping Fang	6
9	Guidelines for Evaluating and Managing Children Born with Disorders of Sexual Development 2012 ·Pediatric Annals ·Ganka Douglas, Marni E. Axelrad, Mary L. Brandt, (unknown), Jennifer E. Dietrich, (unknown), Sheila Gunn, Lefkothea Karaviti, Mónica E. López, Charles G. Macias, Laurence B. McCullough, (unknown), (unknown), V. Reid Sutton	9
10	Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis 2011 ·Molecular Genetics and Metabolism ·Guo-Li Wang, Jing Wang, Ganka Douglas, Marsha F. Browning, Sihoun Hahn, Jaya Ganesh, Sarah K. Cox, Kirk Aleck, Eric Schmitt, Victor Wei Zhang, Lee-Jun Wong	23
11	Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes 2010 ·PLoS ONE ·Bekim Sadiković, Jing Wang, Ayman W. El‐Hattab, Megan Landsverk, Ganka Douglas, Ellen K. Brundage, William J. Craigen, Eric Schmitt, Lee‐Jun C. Wong	41
12	Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team 2010 ·International Journal of Pediatric Endocrinology ·Ganka Douglas, Marni E. Axelrad, Mary L. Brandt, (unknown), Jennifer E. Dietrich, (unknown), Sheila Gunn, Lefkothea Karaviti, Mónica E. López, Charles G. Macias, Laurence B. McCullough, (unknown), V. Reid Sutton	30
13	Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team 2010 ·International Journal of Pediatric Endocrinology ·Ganka Douglas, (unknown), (unknown), (unknown), (unknown), (unknown), Sheila Gunn, Lefkothea Karaviti, (unknown), (unknown), (unknown), (unknown), (unknown)	20

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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