Margaret N. Berry

535 total citations
15 papers, 275 citations indexed

About

Margaret N. Berry is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Epidemiology. According to data from OpenAlex, Margaret N. Berry has authored 15 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 5 papers in Epidemiology. Recurrent topics in Margaret N. Berry's work include Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Coronary Artery Anomalies (5 papers). Margaret N. Berry is often cited by papers focused on Congenital heart defects research (6 papers), Congenital Heart Disease Studies (5 papers) and Coronary Artery Anomalies (5 papers). Margaret N. Berry collaborates with scholars based in United States, United Kingdom and Australia. Margaret N. Berry's co-authors include Vandana Shashi, Matcheri S. Keshavan, Thomas R. Kwapil, Mark J. Pettenati, Timothy D. Howard, César Santos, Kathryn E. Lewandowski, Michael H. Hines, Kelly Schoch and Thomas C. Hart and has published in prestigious journals such as NeuroImage, The American Journal of Human Genetics and Psychiatry Research.

In The Last Decade

Margaret N. Berry

14 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Margaret N. Berry United States	9	182	109	64	61	37	15	275
Molly B. Sheridan United States	8	118 0.6×	137 1.3×	98 1.5×	18 0.3×	30 0.8×	11	281
Rani Sachdev Australia	7	137 0.8×	110 1.0×	24 0.4×	25 0.4×	30 0.8×	26	237
Shay Ben‐Shachar Israel	12	148 0.8×	54 0.5×	59 0.9×	53 0.9×	35 0.9×	26	394
Elke Hobbiebrunken Germany	8	133 0.7×	76 0.7×	31 0.5×	45 0.7×	34 0.9×	11	268
Christian Wentzel Sweden	7	196 1.1×	188 1.7×	28 0.4×	45 0.7×	112 3.0×	8	373
Maria Accadia Italy	14	136 0.7×	116 1.1×	37 0.6×	29 0.5×	19 0.5×	34	421
Nandita Mukhopadhyay United States	11	116 0.6×	220 2.0×	9 0.1×	20 0.3×	29 0.8×	21	354
Rogelio Simón Spain	9	41 0.2×	41 0.4×	37 0.6×	30 0.5×	13 0.4×	19	192
Sharron Townshend Australia	10	85 0.5×	197 1.8×	68 1.1×	13 0.2×	44 1.2×	13	320
Tomi L. Toler United States	7	105 0.6×	139 1.3×	58 0.9×	13 0.2×	50 1.4×	10	275

Countries citing papers authored by Margaret N. Berry

Since Specialization

Citations

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

Fields of papers citing papers by Margaret N. Berry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margaret N. Berry. 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 Margaret N. Berry. The network helps show where Margaret N. Berry may publish in the future.

Co-authorship network of co-authors of Margaret N. Berry

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

All Works

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15 of 15 papers shown

Shashi, Vandana, Pingxing Xie, Kelly Schoch, et al.. (2014). The RBMX gene as a candidate for the Shashi X‐linked intellectual disability syndrome. Clinical Genetics. 88(4). 386–390. 28 indexed citations

Scurr, Ingrid, Louise C. Wilson, Melissa Lees, et al.. (2011). Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype. American Journal of Medical Genetics Part A. 155(3). 508–518. 54 indexed citations

Shashi, Vandana, Timothy D. Howard, Matcheri S. Keshavan, et al.. (2010). COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome. Psychiatry Research. 178(2). 433–436. 16 indexed citations

Shashi, Vandana, Thomas R. Kwapil, Margaret N. Berry, et al.. (2009). Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome. Psychiatry Research Neuroimaging. 181(1). 1–8. 41 indexed citations

Shashi, Vandana, Margaret N. Berry, & Matcheri S. Keshavan. (2009). Mechanistic Approach to Understanding Psychosis Risk in Velocardiofacial Syndrome. Current Pediatric Reviews. 5(2). 89–104. 4 indexed citations

Shashi, Vandana, César Santos, Margaret N. Berry, et al.. (2004). Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. NeuroImage. 21(4). 1399–1406. 42 indexed citations

Shashi, Vandana, Margaret N. Berry, & Michael H. Hines. (2003). Vasomotor instability in neonates with chromosome 22q11 deletion syndrome. American Journal of Medical Genetics Part A. 121A(3). 231–234. 15 indexed citations

Shashi, Vandana, Margaret N. Berry, & Wesley Covitz. (2002). A combination of physical examination and ECG detects the majority of hemodynamically significant heart defects in neonates with Down syndrome. American Journal of Medical Genetics. 108(3). 205–208. 7 indexed citations

Pettenati, Mark J., et al.. (2001). Prenatal diagnosis of complete sole trisomy 1q. Prenatal Diagnosis. 21(6). 435–440. 19 indexed citations

10.

Shashi, Vandana, et al.. (2000). A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27. The American Journal of Human Genetics. 66(2). 469–479. 22 indexed citations

11.

Shashi, Vandana, et al.. (1999). Partial duplication of 4q12q13 leads to a mild phenotype. American Journal of Medical Genetics. 86(1). 51–53. 20 indexed citations

12.

Pettenati, Mark J., et al.. (1999). Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism. Prenatal Diagnosis. 19(1). 25–28.

13.

Shashi, Vandana, et al.. (1999). Partial duplication of 4q12q13 leads to a mild phenotype. American Journal of Medical Genetics. 86(1). 51–53. 1 indexed citations

14.

Pettenati, Mark J., et al.. (1999). Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism. Prenatal Diagnosis. 19(1). 25–28. 4 indexed citations

15.

Thomas, I. T., et al.. (1993). Najjar syndrome revisited. American Journal of Medical Genetics. 47(8). 1151–1152. 2 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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