Nance We

637 total citations
38 papers, 498 citations indexed

About

Nance We is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Experimental and Cognitive Psychology. According to data from OpenAlex, Nance We has authored 38 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Experimental and Cognitive Psychology. Recurrent topics in Nance We's work include Assisted Reproductive Technology and Twin Pregnancy (6 papers), Cognitive Abilities and Testing (6 papers) and Metabolism and Genetic Disorders (4 papers). Nance We is often cited by papers focused on Assisted Reproductive Technology and Twin Pregnancy (6 papers), Cognitive Abilities and Testing (6 papers) and Metabolism and Genetic Disorders (4 papers). Nance We collaborates with scholars based in United States, Spain and Japan. Nance We's co-authors include Irene A. Uchida, David Bixler, Mette Warburg, Ann T. Sweeney, RE Harris, j. c. christian, Mustafa Tekin, Witkop Cj, H. Krieger and John K. Hewitt and has published in prestigious journals such as The American Journal of Human Genetics, Clinical Genetics and PubMed.

In The Last Decade

Nance We

38 papers receiving 458 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nance We United States	12	205	185	115	53	42	38	498
Jeffrey M. Lieblich United States	10	207 1.0×	162 0.9×	35 0.3×	12 0.2×	52 1.2×	12	632
Roger E. Johnsonbaugh United States	13	194 0.9×	127 0.7×	72 0.6×	44 0.8×	82 2.0×	34	610
Silvia Souza da Costa Brazil	17	370 1.8×	397 2.1×	94 0.8×	36 0.7×	22 0.5×	64	740
N. Lucarini Italy	15	212 1.0×	155 0.8×	120 1.0×	40 0.8×	53 1.3×	59	618
Antonia Paula Marques‐de‐Faria Brazil	15	383 1.9×	391 2.1×	75 0.7×	16 0.3×	41 1.0×	51	617
Ellen Taub Israel	8	207 1.0×	263 1.4×	88 0.8×	19 0.4×	24 0.6×	12	446
Ann Hever United Kingdom	5	414 2.0×	182 1.0×	92 0.8×	28 0.5×	81 1.9×	6	651
Ewa Jamroz Poland	13	241 1.2×	139 0.8×	83 0.7×	23 0.4×	35 0.8×	52	529
Gerald J. Bargman United States	11	179 0.9×	164 0.9×	93 0.8×	16 0.3×	38 0.9×	25	474
Aron J. Diament Brazil	14	214 1.0×	152 0.8×	127 1.1×	19 0.4×	47 1.1×	59	561

Countries citing papers authored by Nance We

Since Specialization

Citations

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

Fields of papers citing papers by Nance We

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nance We

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

1.

Tekin, Mustafa, Hatice Akay, Suat Fítöz, et al.. (2008). Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. Clinical Genetics. 73(6). 554–565. 41 indexed citations

2.

Labay, Valentina, Gema Garrido, Anne C. Madeo, et al.. (2007). Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA^Ser(UCN) in sensorineural hearing loss. Clinical Genetics. 73(1). 50–54. 11 indexed citations

3.

Tekin, Mustafa, et al.. (2001). W44C mutation in the connexin 26 gene associated with dominant non‐syndromic deafness. Clinical Genetics. 59(4). 269–273. 18 indexed citations

4.

We, Nance, Joann Bodurtha, John K. Hewitt, et al.. (1998). Models for the longitudinal genetic analysis of same-age twins: application to HDL cholesterol. Twin Research. 1(1). 3–8. 19 indexed citations

5.

We, Nance, Joann Bodurtha, John K. Hewitt, et al.. (1998). Models for the longitudinal genetic analysis of same-age twins: application to HDL cholesterol. Twin Research. 1(1). 3–8. 10 indexed citations

6.

We, Nance, et al.. (1984). Genetic studies of ocular albinism in a large Virginia kindred.. PubMed. 16(2). 183–5, 188. 16 indexed citations

7.

We, Nance. (1982). Genetic analysis of continuous qualitative and multivariate traits in the families of twins.. PubMed. 103 Pt A. 351–63. 2 indexed citations

8.

We, Nance. (1981). Malformations unique to the twinning process.. PubMed. 69A. 123–33. 20 indexed citations

9.

Golden, Wendy L., et al.. (1980). The MZ half-sib design: an approach for the examination of the etiology of congenital malformations.. PubMed. 46. 437–54. 5 indexed citations

10.

We, Nance. (1979). The role of twin studies in human quantitative genetics.. PubMed. 3. 73–107. 11 indexed citations

11.

We, Nance, et al.. (1978). Analysis of serum amino acid levels by the twin study method and comparison with family studies.. PubMed. 24 Pt C. 157–63. 2 indexed citations

12.

We, Nance, et al.. (1978). Evidence for genetic factors influencing serum uric acid levels in man.. PubMed. 24 Pt C. 187–92. 3 indexed citations

13.

We, Nance, et al.. (1978). The inheritance of immunoglobulin levels.. PubMed. 24 Pt C. 171–6. 3 indexed citations

14.

We, Nance. (1977). Quantitative studies of glucose-6-phosphate dehydrogenase.. The American Journal of Human Genetics. 29(5). 537–44. 10 indexed citations

15.

Bixler, David, et al.. (1974). Popliteal pterygium syndrome in monozygous twins.. PubMed. 10(5). 167–75. 1 indexed citations

16.

We, Nance, et al.. (1971). Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.. PubMed. 7(3). 125–8. 8 indexed citations

17.

We, Nance. (1971). Anencephaly and spina bifida: an etiologic hypothesis.. PubMed. 7(1). 97–102. 9 indexed citations

18.

We, Nance, et al.. (1965). Human blood pressure and the ABO blood group system: an apparent association.. PubMed. 37(3). 238–44. 16 indexed citations

19.

We, Nance & Irene A. Uchida. (1964). TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.. PubMed. 16. 380–92. 47 indexed citations

20.

We, Nance. (1962). Hypersplenism in Laennec's cirrhosis.. PubMed. 13. 63–7. 1 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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