Margaret Au

2.3k total citations
23 papers, 840 citations indexed

About

Margaret Au is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Margaret Au has authored 23 papers receiving a total of 840 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Reproductive Medicine. Recurrent topics in Margaret Au's work include Hypothalamic control of reproductive hormones (8 papers), Sexual Differentiation and Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Margaret Au is often cited by papers focused on Hypothalamic control of reproductive hormones (8 papers), Sexual Differentiation and Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Margaret Au collaborates with scholars based in United States, United Kingdom and Switzerland. Margaret Au's co-authors include William F. Crowley, Nelly Pitteloud, Lacey Plummer, Stephanie B. Seminara, Andrew Dwyer, Virginia Hughes, Gerasimos P. Sykiotis, Richard Quinton, Janet E. Hall and James F. Gusella and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Endocrine Reviews.

In The Last Decade

Margaret Au

22 papers receiving 816 citations

Peers

Countries citing papers authored by Margaret Au

Since Specialization

Citations

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

Fields of papers citing papers by Margaret Au

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margaret Au. 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 Margaret Au. The network helps show where Margaret Au may publish in the future.

Co-authorship network of co-authors of Margaret Au

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	ACTC1 Variants Result in Isolated and Syndromic Cardiac Phenotypes 2025 ·Clinical Genetics ·Yuri A. Zárate, (unknown), (unknown), Andrew White, (unknown), Margaret Au, Jing Chen, K. Nicole Weaver, Konstantin V. Korotkov, Emilia Galperin	0
2	Evaluating co‐created patient‐facing materials to increase understanding of genetic test results 2020 ·Journal of Genetic Counseling ·Andrew Dwyer, Margaret Au, Neil Smith, Lacey Plummer, Margaret Lippincott, Ravikumar Balasubramanian, Stephanie B. Seminara	24
3	When moments matter: Finding answers with rapid exome sequencing 2019 ·Molecular Genetics & Genomic Medicine ·Zöe Powis, Kelly D. Farwell Hagman, Kirsten Blanco, Margaret Au, John M. Graham, Kathryn Singh, Natalie M. Gallant, Linda M. Randolph, Meghan C. Towne, Jesse M. Hunter, Deepali N. Shinde, Erika Palmaer, (unknown), Sha Tang	9
4	A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity 2019 ·Neurogenetics ·David B. Beck, T. Subramanian, S. Vijayalingam, (unknown), Sandra Donkervoort, Michele Yang, Holly Dubbs, Xilma R. Ortiz‐González, Shenela Lakhani, Devorah Segal, Margaret Au, John M. Graham, Sumit Verma, Darrel Waggoner, Marwan Shinawi, Carsten G. Bönnemann, Wendy K. Chung, G. Chinnadurai	14
5	Non-Cystic Fibrosis−Related Meconium Ileus: GUCY2C-Associated Disease Discovered through Rapid Neonatal Whole-Exome Sequencing 2019 ·The Journal of Pediatrics ·Jeremy D. Woods, (unknown), Pedro A. Sanchez‐Lara, Margaret Au, Charles F. Simmons, John M. Graham	6
6	FARS2 mutations presenting with pure spastic paraplegia and lesions of the dentate nuclei 2018 ·Annals of Clinical and Translational Neurology ·(unknown), (unknown), Margaret Au, John M. Graham, Noriko Salamon, Michael Ibba, Tyler Mark Pierson	13
7	GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function 2017 ·Journal of Human Genetics ·Wenjuan Chen, Christine Shieh, Sharon A. Swanger, Anel Tankovic, Margaret Au, Marianne McGuire, Michele Tagliati, John M. Graham, Suneeta Madan‐Khetarpal, Stephen F. Traynelis, Hongjie Yuan, Tyler Mark Pierson	59
8	A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families 2016 ·Journal of Molecular Diagnostics ·(unknown), Jonathan D. Buckley, Pedro A. Sanchez‐Lara, Dennis T. Maglinte, (unknown), Tatiana V. Tatarinova, Jennifer G. Aparicio, Jonathan W. Kim, Margaret Au, Dejerianne Ostrow, Thomas C. Lee, Maurice R.G. O’Gorman, Alexander R. Judkins, David Cobrinik, Timothy J. Triche	25
9	When Genetic Load Does Not Correlate with Phenotypic Spectrum: Lessons from the GnRH Receptor (GNRHR) 2012 ·The Journal of Clinical Endocrinology & Metabolism ·Elena Gianetti, Janet E. Hall, Margaret Au, Ursula B. Kaiser, Richard Quinton, Jane A. Stewart, Daniel L. Metzger, Nelly Pitteloud, Verónica Mericq, Paulina M. Merino, Lynne L. Levitsky, Louise Izatt, Mariarosaria Lang‐Muritano, Victor Y. Fujimoto, Robert G. Dluhy, (unknown), William F. Crowley, Lacey Plummer, Stephanie B. Seminara	34
10	Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications 2011 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Virginia Hughes, Lacey Plummer, Margaret Au, Richard L. Doty, Stephanie B. Seminara, Yee-Ming Chan, Nelly Pitteloud, William F. Crowley, Ravikumar Balasubramanian	79
11	Genetic counseling for isolated GnRH deficiency 2011 ·Molecular and Cellular Endocrinology ·Margaret Au, William F. Crowley, Cassandra Buck	28
12	Expanding the Phenotype and Genotype of Female GnRH Deficiency 2011 ·The Journal of Clinical Endocrinology & Metabolism ·Natalie D. Shaw, Stephanie B. Seminara, Corrine K. Welt, Margaret Au, Lacey Plummer, Virginia Hughes, Andrew Dwyer, Kathryn A. Martin, Richard Quinton, Verónica Mericq, Paulina M. Merino, James F. Gusella, William F. Crowley, Nelly Pitteloud, Janet E. Hall	74
13	Expanding the Phenotype and Genotype of Female GnRH Deficiency 2011 ·Endocrinology ·Natalie D. Shaw, (unknown), (unknown), Margaret Au, Lacey Plummer, Virginia Hughes, Andrew Dwyer, Kathryn A. Martin, Richard Quinton, Verónica Mericq, Paulina M. Merino, James F. Gusella, William F. Crowley, Nelly Pitteloud, Janet E. Hall	2
14	Congenital Idiopathic Hypogonadotropic Hypogonadism: Evidence of Defects in the Hypothalamus, Pituitary, and Testes 2010 ·The Journal of Clinical Endocrinology & Metabolism ·Gerasimos P. Sykiotis, (unknown), Magdalena Avbelj Stefanija, Frances J. Hayes, Apisadaporn Thambundit, Andrew Dwyer, Margaret Au, Lacey Plummer, William F. Crowley, Nelly Pitteloud	81
15	Familial risk for chronic disease and intent to share family history with a health care provider among urban Appalachian women, southwestern Ohio, 2007. 2010 ·SHILAP Revista de lepidopterología ·Margaret Au, (unknown), Todd G. Nick, (unknown), Yu Wang, Nancy Steinberg Warren, Melanie F. Myers	7
16	The Role of the Prokineticin 2 Pathway in Human Reproduction: Evidence from the Study of Human and Murine Gene Mutations 2010 ·Endocrine Reviews ·Cecilia Martin, Ravikumar Balasubramanian, Andrew Dwyer, Margaret Au, Yisrael Sidis, Ursula B. Kaiser, Stephanie B. Seminara, Nelly Pitteloud, Qun‐Yong Zhou, William F. Crowley	86
17	Oligogenic basis of isolated gonadotropin-releasing hormone deficiency 2010 ·Proceedings of the National Academy of Sciences ·Gerasimos P. Sykiotis, Lacey Plummer, Virginia Hughes, Margaret Au, (unknown), (unknown), Andrew Dwyer, Richard Quinton, Janet E. Hall, James F. Gusella, Stephanie B. Seminara, William F. Crowley, Nelly Pitteloud	240
18	A Family History Demonstration Project Among Women in an Urban Appalachian Community 2009 ·Progress in community health partnerships ·(unknown), (unknown), (unknown), (unknown), Cynthia A. Prows, (unknown), Nancy Steinberg Warren, Margaret Au, (unknown), (unknown), (unknown), (unknown), (unknown), Jennifer Walters, Melanie F. Myers	17
19	Decisions to Seek Healthcare Based on Family Health History Among Urban Appalachian Women 2009 ·Journal of Genetic Counseling ·Robyn A. Cree, John Lynch, Margaret Au, Melanie F. Myers	9
20	In vivo characterization of transplanted human embryonic stem cell‐derived pancreatic endocrine islet cells 2008 ·Cell Proliferation ·(unknown), Jianming Jiang, Margaret Au, R. V. Rajotte, Kuang‐Hui Lu, Jane Lebkowski, A. S. Majumdar, Gregory S. Korbutt	26

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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