Mary‐Alice Abbott

1.5k total citations
19 papers, 516 citations indexed

About

Mary‐Alice Abbott is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mary‐Alice Abbott has authored 19 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Surgery. Recurrent topics in Mary‐Alice Abbott's work include Prenatal Screening and Diagnostics (3 papers), Lysosomal Storage Disorders Research (3 papers) and Mitochondrial Function and Pathology (2 papers). Mary‐Alice Abbott is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Lysosomal Storage Disorders Research (3 papers) and Mitochondrial Function and Pathology (2 papers). Mary‐Alice Abbott collaborates with scholars based in United States, United Kingdom and Netherlands. Mary‐Alice Abbott's co-authors include Justin R. Fallon, David G. Wells, Priya S. Kishnani, Robert M. Greenstein, Elizabeth K. Schorry, Craig Lapin, Arnold Reuser, Teresa A. Smolarek, Ankita Patel and Dorothy Wakefield and has published in prestigious journals such as Circulation, Journal of Neuroscience and Diabetes.

In The Last Decade

Mary‐Alice Abbott

17 papers receiving 499 citations

Peers

Countries citing papers authored by Mary‐Alice Abbott

Since Specialization

Citations

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

Fields of papers citing papers by Mary‐Alice Abbott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary‐Alice Abbott. 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 Mary‐Alice Abbott. The network helps show where Mary‐Alice Abbott may publish in the future.

Co-authorship network of co-authors of Mary‐Alice Abbott

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Prenatal diagnosis of Hartsfield syndrome with a novel genetic variant 2023 ·Prenatal Diagnosis ·(unknown), Bradley W. Schroeder, (unknown), Mary‐Alice Abbott	2
2	Case report: MELAS and concomitant presumed antiphospholipid antibody syndrome in an adult woman 2022 ·Frontiers in Neurology ·(unknown), (unknown), Richard E. Hicks, Mary‐Alice Abbott, Dennis P. O’Brien, Gottfried Schlaug	1
3	The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene 2021 ·Clinical Genetics ·Servi J.C. Stevens, Constance T. R. M. Stumpel, Karin E. M. Diderich, Marjon A. van Slegtenhorst, Mary‐Alice Abbott, (unknown), Jorune Balciuniene, Louise C. Pyle, Jacqueline Leonard, Jill R. Murrell, (unknown), Iris A.L.M. van Rooij, Alexander Hoischen, Paul Lasko, Han G. Brunner	6
4	Rejecting Gargoylism: Reflections on the term and its relationship to Hurler syndrome 2021 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Mary‐Alice Abbott, (unknown), Sally Rosengren	0
5	Massachusetts’ Findings from Statewide Newborn Screening for Spinal Muscular Atrophy 2021 ·International Journal of Neonatal Screening ·Jaime E. Hale, Basil T. Darras, Kathryn J. Swoboda, Elicia Estrella, (unknown), Mary‐Alice Abbott, Beverly N. Hay, (unknown), (unknown), (unknown), Inderneel Sahai, Roger B. Eaton, Anne Marie Comeau	20
6	GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry 2019 ·Human Mutation ·Arnold Reuser, Ans T. van der Ploeg, Yin‐Hsiu Chien, Juan Clinton Llerena, Mary‐Alice Abbott, Paula R. Clemens, Virginia Kimonis, Nancy Leslie, Sonia S. Maruti, Bernd‐Jan Sanson, (unknown), Magali Periquet, António Toscano, Priya S. Kishnani, (unknown)	53
7	Non-invasive Prenatal Testing (NIPT) 2019 ·(unknown), Mary‐Alice Abbott	0
8	Apparent Mineralocorticoid Excess in the Pediatric Population: Report of a Novel Pathogenic Variant of the 11β-HSD2 Gene and Systematic Review of the Literature. 2019 ·PubMed ·(unknown), (unknown), Anna Tsirka, Mary‐Alice Abbott, Paul Visintainer, Ksenia N. Tonyushkina	3
9	Hydroxysteroid 17-Beta Dehydrogenase Type 10 Disease in Siblings 2016 ·JIMD Reports ·Annely M. Richardson, Gerard T. Berry, Cheryl Garganta, Mary‐Alice Abbott	9
10	Cleft Lip and Palate 2014 ·Pediatrics in Review ·Mary‐Alice Abbott	6
11	Atypical immunologic response in a patient with CRIM-negative Pompe disease 2011 ·Molecular Genetics and Metabolism ·Mary‐Alice Abbott, Sean N. Prater, Suhrad G. Banugaria, Susan Richards, Sarah P. Young, Amy S. Rosenberg, Priya S. Kishnani	24
12	Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping 2009 ·Human Genetics ·Ayman W. El‐Hattab, Teresa A. Smolarek, (unknown), Elizabeth K. Schorry, LaDonna Immken, Gayle Patel, Mary‐Alice Abbott, Brendan C. Lanpher, Zhishuo Ou, Sung‐Hae Kang, Ankita Patel, Fernando Scaglia, James R. Lupski, Sau Wai Cheung, Paweł Stankiewicz	56
13	Improved pulmonary and growth outcomes in cystic fibrosis by newborn screening 2008 ·Pediatric Pulmonology ·(unknown), Mary‐Alice Abbott, Dorothy Wakefield, Craig Lapin, (unknown), Sidney M. Hopfer, Robert M. Greenstein, Michelle M. Cloutier	29
14	The von Hippel–Lindau (VHL) germline mutation V84L manifests as early‐onset bilateral pheochromocytoma 2006 ·American Journal of Medical Genetics Part A ·Mary‐Alice Abbott, Katherine L. Nathanson, Simon Nightingale, Eamonn R. Maher, Robert M. Greenstein	17
15	Liver-Intestine Transplant from a Pediatric Donor with Unrecognized Mitochondrial Succinate Cytochrome C Reductase Deficiency 2005 ·Transplantation ·Aaron R. Zucker, Gabriel Gondolesi, Mary‐Alice Abbott, Robert W. Decker, Sally Rosengren, Thomas Fishbein	5
16	Prenatal genetic diagnosis of Down’s syndrome 2002 ·Expert Review of Molecular Diagnostics ·Mary‐Alice Abbott, Peter Benn	3
17	The Insulin Receptor Tyrosine Kinase Substrate p58/53 and the Insulin Receptor Are Components of CNS Synapses 1999 ·Journal of Neuroscience ·Mary‐Alice Abbott, David G. Wells, Justin R. Fallon	262
18	Familial atrioventricular heart block; an autosomal dominant trait. 1975 ·Circulation ·(unknown), (unknown), (unknown), Eugene Downar, David M. Silver, Mary‐Alice Abbott	19
19	A Clinical Assessment of Fetal Calf Insulin 1961 ·Diabetes ·James Salter, O. V. Sirek, Mary‐Alice Abbott, B. S. Leibel	1

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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