Angela E. Lin

16.3k citations

190 papers · 8.6k indexed · 1 hit paper · h-index 48

Impact in

Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Congenital Ear and Nasal Anomalies
Pediatrics, Perinatology and Child Health top 0.5%
- Prenatal Screening and Diagnostics

Papers in ⓘ

Genetics 74
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 21
- Connective tissue disorders research 15
Pediatrics, Perinatology and Child Health 34
- Prenatal Screening and Diagnostics 21

Co-authors: Lewis B. Holmes (11 shared papers)Allen A. Mitchell (8 shared papers)Sonja A. Rasmussen (7 shared papers)Karen W. Gripp (14 shared papers)John M. Graham (7 shared papers)Tiffany Riehle‐Colarusso (7 shared papers)Lorenzo D. Botto (6 shared papers)Martha M. Werler (5 shared papers)
Journals: Birth Defects Research Part A Clinical and Molecular Teratology (11 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (9 papers)Birth Defects Research (8 papers)PEDIATRICS (6 papers)Genetics in Medicine (6 papers)
Partner nations: United States Italy Canada

In The Last Decade

Angela E. Lin

182 papers receiving 8.4k citations

Hit Papers

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Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting 2017 · 663 citations

Peers

Countries citing papers authored by Angela E. Lin

Since Specialization

Citations

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

Fields of papers citing papers by Angela E. Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Angela E. Lin. 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 Angela E. Lin. The network helps show where Angela E. Lin may publish in the future.

Co-authors

The 25 scholars most cited alongside Angela E. Lin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Angela E. Lin Line = papers co-authored together Angela E. Lin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 190 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting European Journal of Endocrinology ·Claus Højbjerg Gravholt, N.H. Andersen, Gerard Conway, Olaf M. Dekkers, Mitchell E. Geffner, Karen O. Klein, Angela E. Lin, Nelly Mauras, Charmian A. Quigley, Karen Rubin, David E. Sandberg, Theo Sas, Michael Silberbach, Viveca Söderström‐Anttila, Kirstine Stochholm, Janielle A van Alfen-van derVelden, Joachim Woelfle, Philippe Backeljauw, Lorie A. Kloda Hit paper breakdown →	2017	663
2	Guidelines for case classification for the national birth defects prevention study Birth Defects Research Part A Clinical and Molecular Teratology ·Sonja A. Rasmussen, Richard S. Olney, Lewis B. Holmes, Angela E. Lin, Kim M. Keppler‐Noreuil, Cynthia A. Moore	2003	487
3	Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies Birth Defects Research Part A Clinical and Molecular Teratology ·Lorenzo D. Botto, Angela E. Lin, Tiffany Riehle‐Colarusso, Sarita Malik, Adolfo Correa	2007	375
4	First-Trimester Use of Selective Serotonin-Reuptake Inhibitors and the Risk of Birth Defects New England Journal of Medicine ·Carol Louik, Angela E. Lin, Martha M. Werler, Sonia Hernández–Dı́az, Allen A. Mitchell	2007	352
5	CHARGE Association: An Update and Review for the Primary Pediatrician Clinical Pediatrics ·Kim Blake, Sandra L. H. Davenport, Bryan D. Hall, Margaret A. Hefner, Roberta A Pagon, Marc S. Williams, Angela E. Lin, John M. Graham	1998	329
6	Recommendations for the Diagnosis and Management of Turner Syndrome¹ The Journal of Clinical Endocrinology & Metabolism ·Paul Saenger, Kerstin Albertsson Wikland, Gerard S. Conway, Mark Davenport, Claus Højbjerg Gravholt, Raymond L. Hintz, Outi Hovatta, Malou Hultcrantz, Kerstin Landin‐Wilhelmsen, Angela E. Lin, B.M. Lippe, Anna Maria Pasquino, Michael B. Ranke, Ron G. Rosenfeld, Michael Silberbach	2001	282
7	Cardiovascular disease in neurofibromatosis 1: Report of the NF1 Cardiovascular Task Force Genetics in Medicine ·Jan M. Friedman, Jack L. Arbiser, Jonathan A. Epstein, David H. Gutmann, Stephen J. Huot, Angela E. Lin, Bruce M. McManus, Bruce R. Korf	2002	277
8	Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation The American Journal of Human Genetics ·Seema R. Lalani, Arsalan M. Safiullah, Susan Fernbach, Karine G. Harutyunyan, Christina Thaller, L. E. Peterson, John D. McPherson, Richard A. Gibbs, Lisa D. White, Margaret A. Hefner, Sandra L. H. Davenport, John M. Graham, Carlos A. Bacino, Nancy L. Glass, Jeffrey A. Towbin, William J. Craigen, Steven R. Neish, Angela E. Lin, John W. Belmont	2006	264
9	Further Delineation of Aortic Dilation, Dissection, and Rupture in Patients With Turner Syndrome PEDIATRICS ·Angela E. Lin, Barbara M. Lippe, Ron G. Rosenfeld	1998	171
10	TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome The American Journal of Human Genetics ·Jeff M. Milunsky, Tom A. Maher, Geping Zhao, Amy E. Roberts, Heather J. Stalker, Roberto T. Zori, Michelle N. Burch, Michele Clemens, John B. Mulliken, Rosemarie Smith, Angela E. Lin	2008	161
11	Reviewing the evidence for mycophenolate mofetil as a new teratogen: Case report and review of the literature American Journal of Medical Genetics Part A ·Marlene Anderka, Angela E. Lin, Dianne Abuelo, Allen A. Mitchell, Sonja A. Rasmussen	2009	151
12	Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1 American Journal of Medical Genetics ·Angela E. Lin, Patricia Birch, Bruce R. Korf, Romano Tenconi, Michihito Niimura, Minna Pöyhönen, Kim Uhas, M. Sigorini, R Virdis, Corrado Romano, E Bonioli, P. Wolkenstein, Enikö K. Pivnick, Marcella Lawrence, Jan M. Friedman, (unknown)	2000	149
13	Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome American Journal of Medical Genetics ·Giovanni Neri, Fiorella Gurrieri, Ginevra Zanni, Angela E. Lin	1998	135
14	HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation American Journal of Medical Genetics Part A ·Karen W. Gripp, Angela E. Lin, Deborah L. Stabley, Linda K. Nicholson, Charles I. Scott, Daniel Doyle, Yoko Aoki, Yoichi Matsubara, Elaine H. Zackai, Pablo Lapunzina, Antonio González‐Meneses, Jennifer Holbrook, Cynthia A. Agresta, Iris L. Gonzalez, Katia Sol‐Church	2005	133
15	Costello syndrome: a Ras/mitogen activated protein kinase pathway syndrome (rasopathy) resulting from HRAS germline mutations Genetics in Medicine ·Karen W. Gripp, Angela E. Lin	2012	123
16	Diagnosis and Management of Infantile Marfan Syndrome PEDIATRICS ·Richard P. Morse, Sol Rockenmacher, Reed E. Pyeritz, Stephen P. Sanders, Frederick R. Bieber, Angela E. Lin, Patrick MacLeod, Bryan D. Hall, John M. Graham	1990	123
17	Laterality defects in the national birth defects prevention study (1998–2007): Birth prevalence and descriptive epidemiology American Journal of Medical Genetics Part A ·Angela E. Lin, Sergey Krikov, Tiffany Riehle‐Colarusso, Jaime L. Frías, John W. Belmont, Marlene Anderka, Tal Geva, Kelly Getz, Lorenzo D. Botto, (unknown)	2014	123
18	Aortic dilation, dissection, and rupture in patients with turner syndrome The Journal of Pediatrics ·Angela E. Lin, Barbara M. Lippe, Mitchell E. Geffner, Antoinette S. Gomes, Juan F. Lois, Catherine W. Barton, Ammon Rosenthal, William F. Friedman	1986	123
19	Heterotaxy: Associated conditions and hospital-based prevalence in newborns Genetics in Medicine ·Angela E. Lin, Baruch S. Ticho, Kara Houde, Marie‐Noel Westgate, Lewis B. Holmes	2000	118
20	Clinical Approach to Genetic Cardiomyopathy in Children Circulation ·Marcy L. Schwartz, Gerald F. Cox, Angela E. Lin, Mark Korson, Antonio R. Pérez‐Atayde, Ronald V. Lacro, Steven E. Lipshultz	1996	109

About Angela E. Lin

Angela E. Lin is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology and Pulmonary and Respiratory Medicine, having authored 190 papers that have together received 8.6k indexed citations. Recurring topics across this work include Congenital Heart Disease Studies (36 papers), Congenital heart defects research (27 papers), Tracheal and airway disorders (22 papers), Prenatal Screening and Diagnostics (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Protein Tyrosine Phosphatases (18 papers), Congenital Anomalies and Fetal Surgery (17 papers) and Connective tissue disorders research (15 papers). The work is most often cited by research in Genetics (2.7k citations), Genetics (933 citations), Pediatrics, Perinatology and Child Health (1.3k citations), Obstetrics and Gynecology (452 citations) and Pulmonary and Respiratory Medicine (1.9k citations). Angela E. Lin has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Lewis B. Holmes, Allen A. Mitchell, Sonja A. Rasmussen, Karen W. Gripp, John M. Graham, Tiffany Riehle‐Colarusso, Lorenzo D. Botto, Martha M. Werler, Richard S. Olney and Kim M. Keppler‐Noreuil. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Birth Defects Research, PEDIATRICS and Genetics in Medicine.

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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