Donald W. Hadley

4.2k total citations
65 papers, 2.7k citations indexed

About

Donald W. Hadley is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Donald W. Hadley has authored 65 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 18 papers in Molecular Biology and 17 papers in Pathology and Forensic Medicine. Recurrent topics in Donald W. Hadley's work include BRCA gene mutations in cancer (24 papers), Genetic factors in colorectal cancer (16 papers) and Family Support in Illness (9 papers). Donald W. Hadley is often cited by papers focused on BRCA gene mutations in cancer (24 papers), Genetic factors in colorectal cancer (16 papers) and Family Support in Illness (9 papers). Donald W. Hadley collaborates with scholars based in United States, Germany and Australia. Donald W. Hadley's co-authors include Jean Jenkins, Laura M. Koehly, Noralane M. Lindor, Gloria M. Petersen, Karen H. Lu, Susan Miesfeldt, Wylie Burke, Patrick M. Lynch, Nancy Press and Anita Y. Kinney and has published in prestigious journals such as JAMA, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Donald W. Hadley

65 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Donald W. Hadley United States	27	1.4k	754	660	530	341	65	2.7k
Graeme Suthers Australia	25	1.2k 0.9×	981 1.3×	718 1.1×	597 1.1×	262 0.8×	57	2.5k
Ans M.W. van den Ouweland Netherlands	29	1.7k 1.2×	1.5k 1.9×	476 0.7×	619 1.2×	256 0.8×	74	3.4k
June A. Peters United States	21	1.1k 0.8×	586 0.8×	232 0.4×	435 0.8×	261 0.8×	66	2.2k
Wendy McKinnon United States	25	1.1k 0.8×	921 1.2×	328 0.5×	403 0.8×	436 1.3×	46	3.3k
Shirley Hodgson United Kingdom	31	1.3k 0.9×	1.7k 2.2×	574 0.9×	791 1.5×	271 0.8×	91	3.4k
Christi J. van Asperen Netherlands	36	2.4k 1.7×	848 1.1×	564 0.9×	818 1.5×	137 0.4×	104	3.4k
Robin L. Bennett United States	31	2.3k 1.6×	764 1.0×	632 1.0×	478 0.9×	158 0.5×	78	4.2k
Cora M. Aalfs Netherlands	24	705 0.5×	473 0.6×	303 0.5×	658 1.2×	264 0.8×	81	1.9k
Susan M. White Australia	33	1.6k 1.1×	1.4k 1.9×	619 0.9×	541 1.0×	266 0.8×	113	3.5k
Wendy S. Meschino Canada	29	1.5k 1.0×	758 1.0×	223 0.3×	223 0.4×	125 0.4×	78	3.0k

Countries citing papers authored by Donald W. Hadley

Since Specialization

Citations

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

Fields of papers citing papers by Donald W. Hadley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Donald W. Hadley. 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 Donald W. Hadley. The network helps show where Donald W. Hadley may publish in the future.

Co-authorship network of co-authors of Donald W. Hadley

This figure shows the co-authorship network connecting the top 25 collaborators of Donald W. Hadley. A scholar is included among the top collaborators of Donald W. Hadley 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 Donald W. Hadley. Donald W. Hadley 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

Do, Jenny, Emory Ryan, Nahid Tayebi, et al.. (2023). An exploration of knowledge, risk perceptions, and communication in a family with multiple genetic risks for Parkinson's disease. Journal of Genetic Counseling. 32(3). 750–757. 1 indexed citations

Burke, Elizabeth A., Lynne A. Wolfe, Brian P. Brooks, et al.. (2020). A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung disease. American Journal of Medical Genetics Part A. 182(5). 1278–1283. 7 indexed citations

Berger, Seth, Karin Weiss, Ariel F. Martinez, et al.. (2017). SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly. Congenital Anomalies. 58(1). 29–32. 10 indexed citations

Kruszka, Paul, Yonit A. Addissie, Donald W. Hadley, et al.. (2016). Muenke syndrome: An international multicenter natural history study. American Journal of Medical Genetics Part A. 170(4). 918–929. 31 indexed citations

Eliezer, Dina, Donald W. Hadley, & Laura M. Koehly. (2014). Exploring psychological responses to genetic testing for Lynch Syndrome within the family context. Psycho-Oncology. 23(11). 1292–1299. 5 indexed citations

Khromykh, Alina, et al.. (2014). Analysis of renal anomalies in VACTERL association. Birth Defects Research Part A Clinical and Molecular Teratology. 100(10). 801–805. 30 indexed citations

Ashida, Sato, et al.. (2011). The Importance of Older Family Members in Providing Social Resources and Promoting Cancer Screening in Families With a Hereditary Cancer Syndrome. The Gerontologist. 51(6). 833–842. 34 indexed citations

Raam, Manu S., Daniel Pineda‐Alvarez, Donald W. Hadley, & Benjamin D. Solomon. (2010). Long-term outcomes of adults with features of VACTERL association. European Journal of Medical Genetics. 54(1). 34–41. 38 indexed citations

Hadley, Donald W., Sato Ashida, Jean Jenkins, et al.. (2010). Generation after generation: Exploring the psychological impact of providing genetic services through a cascading approach. Genetics in Medicine. 12(12). 808–815. 10 indexed citations

10.

Ersig, Anne L., Donald W. Hadley, & Laura M. Koehly. (2009). Colon cancer screening practices and disclosure after receipt of positive or inconclusive genetic test results for hereditary nonpolyposis colorectal cancer. Cancer. 115(18). 4071–4079. 12 indexed citations

11.

Lindor, Noralane M., Gloria M. Petersen, Donald W. Hadley, et al.. (2006). Recommendations for the Care of Individuals With an Inherited Predisposition to Lynch Syndrome. JAMA. 296(12). 1507–1507. 2 indexed citations

12.

McInerney‐Leo, Aideen, Donald W. Hadley, Katrina Gwinn, & John Hardy. (2004). Genetic testing in Parkinson's disease. Movement Disorders. 20(1). 1–10. 42 indexed citations

13.

Hadley, Donald W., Jean Jenkins, Eileen Dimond, et al.. (2003). Genetic Counseling and Testing in Families With Hereditary Nonpolyposis Colorectal Cancer. Archives of Internal Medicine. 163(5). 573–573. 124 indexed citations

14.

Ng, David, Donald W. Hadley, Cynthia J. Tifft, & Leslie G. Biesecker. (2002). Genetic heterogeneity of syndromic X‐linked recessive microphthalmia‐anophthalmia: Is Lenz microphthalmia a single disorder?. American Journal of Medical Genetics. 110(4). 308–314. 19 indexed citations

15.

Ho, Nicola C., Donald W. Hadley, Pawan Kumar Jain, & Clair A. Francomano. (2002). Case 47: Dural Ectasia Associated with Marfan Syndrome. Radiology. 223(3). 767–771. 18 indexed citations

16.

Peters, Kathryn F., et al.. (2001). The Human Genome Project: An Update. Cancer Nursing. 24(4). 287–292. 6 indexed citations

17.

Gropman, Andrea, Sondra W. Levin, Lynne Yao, et al.. (2000). Unusual renal features of Lowe syndrome in a mildly affected boy. American Journal of Medical Genetics. 95(5). 461–466. 23 indexed citations

18.

Lerman, Caryn, Chanita Hughes, Judith Benkendorf, et al.. (1999). Racial differences in testing motivation and psychological distress following pretest education for BRCA1 gene testing.. PubMed. 8(4 Pt 2). 361–7. 127 indexed citations

19.

Coon, Hilary, M. Hoff, John Holik, et al.. (1996). Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression. Biological Psychiatry. 39(8). 689–696. 42 indexed citations

20.

Hadley, Donald W., M. Hoff, John Holik, et al.. (1995). Manic-Depression and the Norepinephrine Transporter Gene. Human Heredity. 45(3). 165–168. 31 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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