Nancy Kramer

1.9k total citations
16 papers, 522 citations indexed

About

Nancy Kramer is a scholar working on Molecular Biology, Genetics and Social Psychology. According to data from OpenAlex, Nancy Kramer has authored 16 papers receiving a total of 522 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Social Psychology. Recurrent topics in Nancy Kramer's work include Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Nancy Kramer is often cited by papers focused on Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Nancy Kramer collaborates with scholars based in United States, United Kingdom and Netherlands. Nancy Kramer's co-authors include John M. Graham, Thane S. Pittman, Karen W. Gripp, Ghayda Mirzaa, Dawn H. Siegel, Elizabeth Hopkins, Dorit Lev, Tally Lerman‐Sagie, Robert L. Conway and Linda S. deVries and has published in prestigious journals such as Journal of the American College of Cardiology, The American Journal of Human Genetics and Personality and Social Psychology Bulletin.

In The Last Decade

Nancy Kramer

15 papers receiving 469 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nancy Kramer United States	11	181	178	92	83	64	16	522
Gabriel Levi United States	16	81 0.4×	98 0.6×	154 1.7×	25 0.3×	34 0.5×	54	766
Beth Solomon United States	13	29 0.2×	136 0.8×	56 0.6×	110 1.3×	12 0.2×	23	889
Katharina Bauer Germany	14	33 0.2×	229 1.3×	20 0.2×	73 0.9×	36 0.6×	33	955
Kelly D. Farwell United States	10	178 1.0×	215 1.2×	28 0.3×	12 0.1×	65 1.0×	11	591
Jeffrey Larson United States	11	59 0.3×	224 1.3×	79 0.9×	37 0.4×	25 0.4×	23	543
Petra G. Frets Netherlands	20	879 4.9×	212 1.2×	52 0.6×	45 0.5×	388 6.1×	32	1.4k
Nicole Wong Australia	14	209 1.2×	562 3.2×	164 1.8×	17 0.2×	36 0.6×	30	1.1k
Michela Vezzoli Italy	13	75 0.4×	282 1.6×	96 1.0×	26 0.3×	11 0.2×	36	731
Anne M. Goodwin United States	9	36 0.2×	430 2.4×	77 0.8×	57 0.7×	5 0.1×	18	824

Countries citing papers authored by Nancy Kramer

Since Specialization

Citations

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

Fields of papers citing papers by Nancy Kramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy Kramer. A scholar is included among the top collaborators of Nancy Kramer 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 Nancy Kramer. Nancy Kramer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Boyle, Lia, Mirjam M. C. Wamelink, Gajja S. Salomons, et al.. (2016). Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects. The American Journal of Human Genetics. 98(6). 1235–1242. 33 indexed citations

Russell, Bianca, Jennifer J. Johnston, Leslie G. Biesecker, et al.. (2015). Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance. American Journal of Medical Genetics Part A. 167(9). 2122–2131. 47 indexed citations

Barber, John, Jill A. Rosenfeld, John M. Graham, et al.. (2015). Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance. American Journal of Medical Genetics Part A. 167(9). 2052–2064. 28 indexed citations

Kramer, Nancy, Charles E. Schwartz, Judith H. Miles, et al.. (2014). 19q13.32 microdeletion syndrome: Three new cases. European Journal of Medical Genetics. 57(11-12). 654–658. 27 indexed citations

Au, Ping Yee Billie, Hilary Racher, John M. Graham, et al.. (2013). De novo exon 1 missense mutations of SKI and Shprintzen‐Goldberg syndrome: Two new cases and a clinical review. American Journal of Medical Genetics Part A. 164(3). 676–684. 11 indexed citations

Kramer, Nancy, et al.. (2013). Central Vascular Access Device Guidelines for Pediatric Home-Based Patients: Driving Best Practices. Journal of the Association for Vascular Access. 18(2). 103–113. 1 indexed citations

Mirzaa, Ghayda, Robert L. Conway, Karen W. Gripp, et al.. (2012). Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis. American Journal of Medical Genetics Part A. 158A(2). 269–291. 121 indexed citations

Shih, Jean C., et al.. (2012). De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine. European Journal of Medical Genetics. 55(5). 349–353. 8 indexed citations

Rosenfeld, Jill A., Brad Angle, Valerie Banks, et al.. (2011). Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25. American Journal of Medical Genetics Part A. 155(6). 1336–1351. 29 indexed citations

10.

Graham, John M., Nancy Kramer, Bassem A. Bejjani, et al.. (2009). Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome. American Journal of Medical Genetics Part A. 149A(10). 2122–2128. 24 indexed citations

11.

Kramer, Nancy, et al.. (2007). The effects of an embodied conversationational agent's subtle nonverbal behavior on user's evaluation and behavioral mimicry. PUB – Publications at Bielefeld University (Bielefeld University). 1 indexed citations

12.

Walder, Roxanne Y., Michael R. Garrett, Gretel Beck, et al.. (1998). Short tandem repeat polymorphic markers for the rat genome from marker-selected libraries. Mammalian Genome. 9(12). 1013–1021. 13 indexed citations

13.

Feld, Steven, Edgar S. Carell, Olle Kjellgren, et al.. (1996). Comparison of angioscopy, intravascular ultrasound imaging and quantitative coronary angiography in predicting clinical outcome after coronary intervention in high risk patients. Journal of the American College of Cardiology. 28(1). 97–105. 43 indexed citations

14.

Pittman, Thane S., et al.. (1980). Informational versus Controlling Verbal Rewards. Personality and Social Psychology Bulletin. 6(2). 228–233. 130 indexed citations

15.

Campbell, Carole A., et al.. (1979). The Social Security Administration's Claims Development and Decision Process. Proceedings of the Human Factors Society Annual Meeting. 23(1). 577–580. 1 indexed citations

16.

Kramer, Nancy, et al.. (1977). Outpatient Group Psychotherapy for the Elderly: An Alternative to Institutionalization. Psychiatric Services. 28(6). 440–442. 5 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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