Anna Newlin

1.9k total citations
17 papers, 425 citations indexed

About

Anna Newlin is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Anna Newlin has authored 17 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Anna Newlin's work include Genetic factors in colorectal cancer (5 papers), BRCA gene mutations in cancer (4 papers) and Genomics and Rare Diseases (3 papers). Anna Newlin is often cited by papers focused on Genetic factors in colorectal cancer (5 papers), BRCA gene mutations in cancer (4 papers) and Genomics and Rare Diseases (3 papers). Anna Newlin collaborates with scholars based in United States and Canada. Anna Newlin's co-authors include Ellen Roy Elias, David H. Ledbetter, William B. Dobyns, Scott M. Weissman, Timothy T. McMahon, Barbara K. Burton, Marilyn T. Miller, Joel Sugar, Timothy B. Edrington and Kristen J. Vogel and has published in prestigious journals such as Neurology, Ophthalmology and Investigative Ophthalmology & Visual Science.

In The Last Decade

Anna Newlin

16 papers receiving 406 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anna Newlin United States	12	210	147	96	65	64	17	425
Hadia Hijazi Saudi Arabia	11	226 1.1×	333 2.3×	84 0.9×	59 0.9×	77 1.2×	15	579
Kristin Bosse Germany	14	312 1.5×	244 1.7×	62 0.6×	22 0.3×	23 0.4×	24	526
Luke St Heaps Australia	10	188 0.9×	214 1.5×	53 0.6×	23 0.4×	28 0.4×	22	379
Anthony Raizis New Zealand	9	136 0.6×	434 3.0×	84 0.9×	12 0.2×	30 0.5×	18	550
Becky Alhadeff United States	13	183 0.9×	374 2.5×	42 0.4×	38 0.6×	11 0.2×	17	538
G. Del Porto Italy	12	186 0.9×	154 1.0×	64 0.7×	15 0.2×	38 0.6×	26	344
Gabi Mücher Germany	10	408 1.9×	474 3.2×	64 0.7×	25 0.4×	10 0.2×	11	609
Carmelilia De Bernardo Italy	16	261 1.2×	336 2.3×	41 0.4×	10 0.2×	24 0.4×	32	612
Sarina Sulong Malaysia	10	73 0.3×	157 1.1×	38 0.4×	11 0.2×	25 0.4×	48	378
Wolfram Heinritz Germany	12	104 0.5×	175 1.2×	21 0.2×	31 0.5×	12 0.2×	28	380

Countries citing papers authored by Anna Newlin

Since Specialization

Citations

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

Fields of papers citing papers by Anna Newlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Newlin

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Newlin. A scholar is included among the top collaborators of Anna Newlin 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 Anna Newlin. Anna Newlin 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:

17 of 17 papers shown

Hampel, Heather, et al.. (2022). Utilizing Public Health Frameworks and Partnerships to Ensure Equity in DNA-Based Population Screening. Frontiers in Genetics. 13. 886755–886755.

Byers, Heather M., Angela Jacobson, Cigdem Ussakli, et al.. (2018). Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives. JCO Precision Oncology. 2(2). 1–7. 1 indexed citations

Stoll, Jessica, Scott M. Weissman, Christina G. Selkirk, et al.. (2016). Evaluation of laboratory perspectives on hereditary cancer panels. Familial Cancer. 15(4). 689–696. 3 indexed citations

Selkirk, Christina G., Kristen J. Vogel, Anna Newlin, et al.. (2014). Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice. Familial Cancer. 13(4). 527–536. 29 indexed citations

Weissman, Scott M., et al.. (2012). Genetic Testing by Cancer Site. The Cancer Journal. 18(4). 320–327. 39 indexed citations

Banks, Kimberly C., Jessica Moline, Monica Marvin, Anna Newlin, & Kristen J. Vogel. (2012). 10 rare tumors that warrant a genetics referral. Familial Cancer. 12(1). 1–18. 22 indexed citations

O’Neill, Suzanne M., Wendy S. Rubinstein, Stephen Sener, et al.. (2008). Psychological impact of recall in high-risk breast MRI screening. Breast Cancer Research and Treatment. 115(2). 365–371. 17 indexed citations

Smith, Jennifer Hasenyager, et al.. (2007). Genetic Study of Familial Uveal Melanoma. Ophthalmology. 114(4). 774–779. 24 indexed citations

Locker, Gershon Y., Karen L. Kaul, David S. Weinberg, et al.. (2006). The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features. Cancer Genetics and Cytogenetics. 169(1). 33–38. 12 indexed citations

10.

Lines, Matthew A., K. Kozlowski, Stephen C. Kulak, et al.. (2004). Characterization and Prevalence ofPITX2Microdeletions and Mutations in Axenfeld-Rieger Malformations. Investigative Ophthalmology & Visual Science. 45(3). 828–828. 53 indexed citations

11.

McMahon, Timothy T., Julie A. Shin, Anna Newlin, et al.. (1999). Discordance for Keratoconus in Two Pairs of Monozygotic Twins. Cornea. 18(4). 444–451. 52 indexed citations

12.

Newlin, Anna, et al.. (1999). Mosaic trisomy 7 in a patient with pigmentary abnormalities. American Journal of Medical Genetics. 87(5). 371–374. 4 indexed citations

13.

Newlin, Anna, et al.. (1999). Mosaic trisomy 7 in a patient with pigmentary abnormalities. American Journal of Medical Genetics. 87(5). 371–374. 31 indexed citations

14.

Leichtman, Lawrence G., Joleen L. Zackowski, Patrick D. Storto, & Anna Newlin. (1996). Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: Case report and comparison with trisomy 9p. American Journal of Medical Genetics. 63(3). 434–437. 16 indexed citations

15.

Brothman, Arthur R., et al.. (1993). Prenatal detection of an inverted X chromosome in a male. Clinical Genetics. 44(3). 139–141. 2 indexed citations

16.

Dobyns, William B., et al.. (1992). Causal heterogeneity in isolated lissencephaly. Neurology. 42(7). 1375–1375. 99 indexed citations

17.

Shaffer, Lisa G., Mary L. Marazita, Joann Bodurtha, Anna Newlin, & W. E. Nance. (1990). Evidence for a major gene in familial anencephaly. American Journal of Medical Genetics. 36(1). 97–101. 21 indexed citations

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