M. Adela Mansilla

2.7k total citations
29 papers, 1.2k citations indexed

About

M. Adela Mansilla is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, M. Adela Mansilla has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Nephrology. Recurrent topics in M. Adela Mansilla's work include Cleft Lip and Palate Research (16 papers), Craniofacial Disorders and Treatments (8 papers) and dental development and anomalies (6 papers). M. Adela Mansilla is often cited by papers focused on Cleft Lip and Palate Research (16 papers), Craniofacial Disorders and Treatments (8 papers) and dental development and anomalies (6 papers). M. Adela Mansilla collaborates with scholars based in United States, Brazil and Denmark. M. Adela Mansilla's co-authors include Jeffrey C. Murray, Mary L. Marazita, Alexandre R. Vieira, Sandra Daack‐Hirsch, Bridget Riley‐Gillis, Brion S. Maher, Margaret E. Cooper, Andrew C. Lidral, Jinghong Ma and Moosa Mohammadi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Genetics.

In The Last Decade

M. Adela Mansilla

27 papers receiving 1.1k citations

Peers

Countries citing papers authored by M. Adela Mansilla

Since Specialization

Citations

This map shows the geographic impact of M. Adela Mansilla'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 M. Adela Mansilla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Adela Mansilla more than expected).

Fields of papers citing papers by M. Adela Mansilla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Adela Mansilla. 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 M. Adela Mansilla. The network helps show where M. Adela Mansilla may publish in the future.

Co-authorship network of co-authors of M. Adela Mansilla

This figure shows the co-authorship network connecting the top 25 collaborators of M. Adela Mansilla. A scholar is included among the top collaborators of M. Adela Mansilla 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 M. Adela Mansilla. M. Adela Mansilla is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Variants of unknown significance are common in brushite stone formers undergoing genetic testing for nephrolithiasis 2025 ·Urolithiasis ·(unknown), (unknown), (unknown), (unknown), (unknown), M. Adela Mansilla, (unknown), Christie P. Thomas, Chad R. Tracy, Ryan L. Steinberg	0
2	Suspected Autosomal Recessive Polycystic Kidney Disease but Cerebellar Vermis Hypoplasia, Oligophrenia Ataxia, Coloboma, and Hepatic Fibrosis (COACH) Syndrome in Retrospect, A Delayed Diagnosis Aided by Genotyping and Reverse Phenotyping: A Case Report and A Review of the Literature 2023 ·The Nephron journals/Nephron journals ·(unknown), (unknown), (unknown), Girish Bathla, (unknown), (unknown), M. Adela Mansilla, Christie P. Thomas	2
3	Familial hyperkalemic hypertension: hyperkalemia not hypertension defines dominant KLHL3 disease and may permit earlier recognition and tailored therapy 2022 ·Journal of Nephrology ·(unknown), Jyothsna Gattineni, Lama Noureddine, M. Adela Mansilla, Christie P. Thomas	0
4	Sequential genetic testing of living‐related donors for inherited renal disease to promote informed choice and enhance safety of living donation 2021 ·Transplant International ·Christie P. Thomas, (unknown), (unknown), (unknown), (unknown), Danniele G. Holanda, Daniel Katz, Benjamin W. Darbro, M. Adela Mansilla, Richard J. Smith	12
5	Minimal Change Disease With Nephrotic Syndrome Associated With Coronavirus Disease 2019 After Apolipoprotein L1 Risk Variant Kidney Transplant: A Case Report 2020 ·Transplantation Proceedings ·(unknown), Prerna Rastogi, Dilek İnce, (unknown), M. Adela Mansilla, Richard J. Smith, Sarat Kuppachi, Christie P. Thomas	15
6	Assessment of sensorimotor intelligence and psychomotor development in clinically healthy infants assisted in the public health sector 2019 ·Archivos Argentinos de Pediatria ·(unknown), (unknown), (unknown), (unknown), M. Adela Mansilla, (unknown), (unknown)	3
7	Ketogenic diet – A novel treatment for early epileptic encephalopathy due to PIGA deficiency 2016 ·Brain and Development ·Charuta Joshi, Diana L. Kolbe, M. Adela Mansilla, (unknown), Richard J. Smith, Colleen A. Campbell	29
8	Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing Strategy 2016 ·American Journal of Transplantation ·Christie P. Thomas, M. Adela Mansilla, Ramakrishna Sompallae, (unknown), (unknown), (unknown), Colleen A. Campbell, Anne E. Kwitek, Benjamin W. Darbro, Zoe A. Stewart, Richard J. Smith	23
9	Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study 2013 ·Human Genetics ·Terri H. Beaty, Margaret A. Taub, Alan F. Scott, Jeffrey C. Murray, Mary L. Marazita, Holger Schwender, Margaret M. Parker, Jacqueline B. Hetmanski, Poojitha Balakrishnan, M. Adela Mansilla, Elisabeth Mangold, Kerstin U. Ludwig, Markus M. Nöethen, Michele Rubini, Nursel Elcioğlu, Ingo Ruczinski	112
10	A Mutation in Mouse Pak1ip1 Causes Orofacial Clefting while Human PAK1IP1 Maps to 6p24 Translocation Breaking Points Associated with Orofacial Clefting 2013 ·PLoS ONE ·(unknown), M. Adela Mansilla, Youngshik Choe, (unknown), Richard A. Sturm, Roy L. Maute, Scott May, Kamil K. Hozyasz, Piotr Wójcicki, Adrianna Mostowska, (unknown), Iannis E. Adamopoulos, Samuel J. Pleasure, Jeffrey C. Murray, Konstantinos S. Zarbalis	40
11	Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome‐wide association on chromosome 1p22 2012 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Elizabeth J. Leslie, M. Adela Mansilla, Leah C. Biggs, (unknown), (unknown), Margaret E. Cooper, Martine Dunnwald, Andrew C. Lidral, Mary L. Marazita, Terri H. Beaty, Jeffrey C. Murray	78
12	Genomic strategy identifies a missense mutation in WD‐repeat domain 65 (WDR65) in an individual with Van der Woude syndrome 2011 ·American Journal of Medical Genetics Part A ·(unknown), Akira Kinoshita, Jason L. Weirather, Myriam Peyrard‐Janvid, Renata Lúcia Leite Ferreira de Lima, Martine Dunnwald, Alan Shanske, Danilo Moretti‐Ferreira, Hannele Koillinen, Juha Kere, M. Adela Mansilla, Jeffrey C. Murray, (unknown), Brian C. Schutte	10
13	Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome 2011 ·The American Journal of Human Genetics ·James O’Sullivan, Carolina Cavalcante Bitu, Sarah B. Daly, Jill Urquhart, Martin Barron, Sanjeev S. Bhaskar, Hercílio Martelli‐Júnior, (unknown), M. Adela Mansilla, Jeffrey C. Murray, Ricardo D. Coletta, Graeme C. Black, Michael J. Dixon	126
14	Autoantibodies to Folate Receptor α During Early Pregnancy and Risk of Oral Clefts in Denmark 2010 ·Pediatric Research ·Camilla Bille, Dorthe Pedersen, Anne‐Marie Nybo Andersen, M. Adela Mansilla, Jeffrey C. Murray, Kaare Christensen, Johnathan Ballard, (unknown), Robert M. Cabrera, Richard H. Finnell	14
15	CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip with or without Cleft Palate 2010 ·The Cleft Palate-Craniofacial Journal ·Ariadne Letra, Renato Menezes, Margaret E. Cooper, (unknown), (unknown), Manika Govil, José Mauro Granjeiro, (unknown), M. Adela Mansilla, Jeffrey C. Murray, Eduardo E. Castilla, Iêda M. Orioli, Andrew E. Czeizel, Lian Ma, Brett Chiquet, Jacqueline T. Hecht, Alexandre R. Vieira, Mary L. Marazita	23
16	Identification of microdeletions in candidate genes for cleft lip and/or palate 2009 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Min Shi, Adrianna Mostowska, Astanand Jugessur, Marla Johnson, M. Adela Mansilla, Kaare Christensen, Rolv T. Lie, Allen J. Wilcox, Jeffrey C. Murray	48
17	Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results 2009 ·Human Heredity ·Mary L. Marazita, Andrew C. Lidral, Jeffrey C. Murray, L. Leigh Field, Brion S. Maher, Toby McHenry, Margaret E. Cooper, Manika Govil, Sandra Daack‐Hirsch, Bridget Riley‐Gillis, Astanand Jugessur, Têmis Maria Félix, (unknown), M. Adela Mansilla, Alexandre R. Vieira, Kim Doheny, Elizabeth Pugh, (unknown), Mauricio Arcos‐Burgos	97
18	The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P 2008 ·European Journal of Human Genetics ·Sun Jin Choi, Mary L. Marazita, P. Suzanne Hart, Paweł Sulima, L. Leigh Field, Toby McHenry, Manika Govil, Margaret E. Cooper, Ariadne Letra, Renato Menezes, Sowmya Narayanan, M. Adela Mansilla, José Mauro Granjeiro, Alexandre R. Vieira, Andrew C. Lidral, Jeffrey C. Murray, Thomas C. Hart	44
19	Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation 2007 ·Journal of Medical Genetics ·Kazutoyo Osoegawa, (unknown), Kagistia Hana Utami, M. Adela Mansilla, Marla Johnson, (unknown), Jamie L’Heureux, Rolph Pfundt, Johan Staaf, (unknown), Andrew C. Lidral, Eric Schoenmakers, Åke Borg, Brian C. Schutte, Edward J. Lammer, Jeffrey C. Murray, Pieter J. de Jong	76
20	Discordant MZ Twins With Cleft Lip and Palate: A Model for Identifying Genes in Complex Traits 2005 ·Twin Research and Human Genetics ·M. Adela Mansilla, (unknown), Laura E. Mitchell, Kaare Christensen, Dorret I. Boomsma, Sandra Daack‐Hirsch, (unknown), Diego F. Wyszynski, Têmis Maria Félix, Nicholas G. Martin, Jeffrey C. Murray	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.

Explore authors with similar magnitude of impact