Theresa Conway

1.7k total citations
32 papers, 1.3k citations indexed

About

Theresa Conway is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Theresa Conway has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Pathology and Forensic Medicine. Recurrent topics in Theresa Conway's work include BRCA gene mutations in cancer (12 papers), Genetic Associations and Epidemiology (10 papers) and Genetic factors in colorectal cancer (8 papers). Theresa Conway is often cited by papers focused on BRCA gene mutations in cancer (12 papers), Genetic Associations and Epidemiology (10 papers) and Genetic factors in colorectal cancer (8 papers). Theresa Conway collaborates with scholars based in United States, China and France. Theresa Conway's co-authors include Hong‐Wen Deng, Robert R. Recker, Henry T. Lynch, Fu‐Hua Xu, K. Michael Davies, Jane F. Lynch, Hui Shen, Patrice Watson, Hongyi Deng and Hongyi Deng and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Cancer and The American Journal of Human Genetics.

In The Last Decade

Theresa Conway

31 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Theresa Conway United States	22	713	508	418	260	234	32	1.3k
Miia Suuriniemi United States	15	181 0.3×	236 0.5×	248 0.6×	196 0.8×	138 0.6×	18	847
Yun-qiu Hu China	17	305 0.4×	363 0.7×	296 0.7×	153 0.6×	215 0.9×	49	878
Dana Gaddy-Kurten United States	14	285 0.4×	491 1.0×	59 0.1×	255 1.0×	23 0.1×	15	1.0k
Young Linda United States	5	208 0.3×	412 0.8×	431 1.0×	483 1.9×	62 0.3×	5	978
Mila Jhamai Netherlands	10	186 0.3×	250 0.5×	174 0.4×	111 0.4×	204 0.9×	13	612
Bruno Ferraz‐de‐Souza Brazil	17	759 1.1×	816 1.6×	47 0.1×	63 0.2×	63 0.3×	35	1.2k
Qiuju Huang Netherlands	7	182 0.3×	289 0.6×	414 1.0×	175 0.7×	241 1.0×	9	794
Jie‐Mei Gu China	17	294 0.4×	312 0.6×	237 0.6×	172 0.7×	208 0.9×	44	888
Fredrik Stiger Sweden	12	135 0.2×	235 0.5×	136 0.3×	126 0.5×	65 0.3×	13	436

Countries citing papers authored by Theresa Conway

Since Specialization

Citations

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

Fields of papers citing papers by Theresa Conway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Theresa Conway

This figure shows the co-authorship network connecting the top 25 collaborators of Theresa Conway. A scholar is included among the top collaborators of Theresa Conway 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 Theresa Conway. Theresa Conway 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

Lynch, Henry T., et al.. (2010). Hereditary ovarian cancer: Heterogeneity in age at onset. Cancer. 71(S2). 573–581. 16 indexed citations

Huang, Qing-Yang, Hui Shen, Hong-Yi Deng, et al.. (2006). Linkage and Association Between CA Repeat Polymorphism of the TNFR2 Gene and Obesity Phenotypes in Two Independent Caucasian Populations. Acta Genetica Sinica. 33(9). 775–781. 1 indexed citations

Huang, Qing-Yang, Hui Shen, Hong-Yi Deng, et al.. (2006). CA repeat polymorphism of the TNFR2 gene is not associated with bone mineral density in two independent Caucasian populations. Journal of Bone and Mineral Metabolism. 24(2). 132–137. 2 indexed citations

Xu, Fu‐Hua, Yong‐Jun Liu, Hongyi Deng, et al.. (2004). A follow-up linkage study for bone size variation in an extended sample. Bone. 35(3). 777–784. 4 indexed citations

Xu, Fu‐Hua, Hui Shen, Yong‐Jun Liu, et al.. (2004). Genetic Dissection of Human Stature in a Large Sample of Multiplex Pedigrees. Annals of Human Genetics. 68(5). 472–488. 30 indexed citations

Liu, Yong‐Jun, Fu‐Hua Xu, Hui Shen, et al.. (2004). A Follow-Up Linkage Study for Quantitative Trait Loci Contributing to Obesity-Related Phenotypes. The Journal of Clinical Endocrinology & Metabolism. 89(2). 875–882. 27 indexed citations

Deng, Hong‐Wen, Hong‐Wen Deng, Hui Shen, et al.. (2003). Several genomic regions potentially containing QTLs for bone size variation were identified in a whole‐genome linkage scan. American Journal of Medical Genetics Part A. 119A(2). 121–131. 36 indexed citations

Deng, Hong‐Wen, Hong‐Wen Deng, Fu‐Hua Xu, et al.. (2002). A whole‐genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature. American Journal of Medical Genetics. 113(1). 29–39. 57 indexed citations

Deng, Hong‐Wen, et al.. (2002). Determination of Bone Size of Hip, Spine, and Wrist in Human Pedigrees by Genetic and Lifestyle Factors. Journal of Clinical Densitometry. 5(1). 45–56. 47 indexed citations

10.

Deng, Hong‐Wen, Hong‐Wen Deng, Michael C. Mahaney, et al.. (2001). Relevance of the genes for bone mass variation to susceptibility to osteoporotic fractures and its implications to gene search for complex human diseases. Genetic Epidemiology. 22(1). 12–25. 106 indexed citations

11.

Deng, Hong‐Wen, Hong‐Wen Deng, Fu‐Hua Xu, et al.. (2001). Is Population Bone Mineral Density Variation Linked to the Marker D11S987 On Chromosome 11q12–13?. The Journal of Clinical Endocrinology & Metabolism. 86(8). 3735–3741. 36 indexed citations

12.

Deng, Hong‐Wen, Hong‐Wen Deng, Wei‐Min Chen, et al.. (2000). Determination of bone mineral density of the hip and spine in human pedigrees by genetic and life-style factors. Genetic Epidemiology. 19(2). 160–177. 97 indexed citations

13.

Conway, Theresa, et al.. (1999). Learning momentum and energy conservation principles with motion detectors and video analysis. APS.

14.

Lynch, Henry T., et al.. (1994). Psychological aspects of monitoring high risk women for breast cancer. Cancer. 74(S3). 1184–1192. 31 indexed citations

15.

Narod, Steven A., Jean Feunteun, Henry T. Lynch, et al.. (1992). Familial Breast-Ovarian Cancer Locus on Chromosome 17q12-q23. Obstetrical & Gynecological Survey. 47(3). 190–190. 32 indexed citations

16.

Lynch, Henry T., Patrice Watson, Theresa Conway, & Jane F. Lynch. (1992). Natural history and age at onset of hereditary breast cancer. Cancer. 69(6). 1404–1407. 18 indexed citations

17.

Lynch, Henry T., Theresa Conway, & Jane Lynch. (1991). Hereditary ovarian cancer. Cancer Genetics and Cytogenetics. 53(2). 161–183. 33 indexed citations

18.

Lynch, Henry T., Mary Lee Fitzsimmons, Theresa Conway, Chhanda Bewtra, & Jane F. Lynch. (1990). Hereditary carcinoma of the ovary and associated cancers: A study of two families. Gynecologic Oncology. 36(1). 48–55. 26 indexed citations

19.

Lynch, Henry T., Patrice Watson, Theresa Conway, & Jane F. Lynch. (1990). Clinical/genetic features in hereditary breast cancer. Breast Cancer Research and Treatment. 15(2). 63–71. 32 indexed citations

20.

Fitzsimmons, Mary Lee, et al.. (1988). Breast cancer diagnosis in a putative obligate gene carrier. Cancer Genetics and Cytogenetics. 36(2). 205–210. 4 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.

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