Barbara R. Pober

9.4k total citations · 1 hit paper
102 papers, 5.0k citations indexed

About

Barbara R. Pober is a scholar working on Developmental Neuroscience, Molecular Biology and Surgery. According to data from OpenAlex, Barbara R. Pober has authored 102 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Developmental Neuroscience, 30 papers in Molecular Biology and 24 papers in Surgery. Recurrent topics in Barbara R. Pober's work include Williams Syndrome Research (49 papers), Congenital Diaphragmatic Hernia Studies (19 papers) and Nuclear Receptors and Signaling (17 papers). Barbara R. Pober is often cited by papers focused on Williams Syndrome Research (49 papers), Congenital Diaphragmatic Hernia Studies (19 papers) and Nuclear Receptors and Signaling (17 papers). Barbara R. Pober collaborates with scholars based in United States, United Kingdom and Canada. Barbara R. Pober's co-authors include Lewis B. Holmes, Martha M. Werler, Kate G. Ackerman, Lucy R. Osborne, Zsolt Urbán, Mauro Longoni, Mark D. Johnson, Patricia K. Donahoe, Angela E. Lin and Meaghan Russell and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Barbara R. Pober

101 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Williams–Beuren Syndrome

2010 540 citations Barbara R. Pober New England Journal of Medicine profile →

Peers

Countries citing papers authored by Barbara R. Pober

Since Specialization

Citations

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

Fields of papers citing papers by Barbara R. Pober

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara R. Pober. 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 Barbara R. Pober. The network helps show where Barbara R. Pober may publish in the future.

Co-authorship network of co-authors of Barbara R. Pober

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara R. Pober. A scholar is included among the top collaborators of Barbara R. Pober 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 Barbara R. Pober. Barbara R. Pober 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

#	Work	Indexed citations
1	Body mass index variation in adults with Williams syndrome: associations with predicted dietary intake and food behaviors 2023 ·Food & Nutrition Research ·(unknown), Takara L. Stanley, Jessica L. Waxler, Hang Lee, Barbara R. Pober, (unknown)	4
2	Williams syndrome 2021 ·Nature Reviews Disease Primers ·Beth A. Kozel, Boaz Barak, Chong Ae Kim, Carolyn Β. Mervis, Lucy R. Osborne, Melanie Porter, Barbara R. Pober	116
3	Attention Bias to Emotional Faces Varies by IQ and Anxiety in Williams Syndrome 2016 ·Journal of Autism and Developmental Disorders ·Lauren M. McGrath, (unknown), Yael G. Dai, Helen F. Dodd, Jessica L. Waxler, Caitlin C. Clements, Sydney Weill, Alison G. Hoffnagle, (unknown), (unknown), Jennifer Mullett, Christopher J. McDougle, Barbara R. Pober, Jordan W. Smoller	18
4	Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes 2012 ·Proceedings of the National Academy of Sciences ·Meaghan Russell, Mauro Longoni, Julie Wells, Faouzi I. Maalouf, Adam Tracy, Marı́a Loscertales, Kate G. Ackerman, Barbara R. Pober, Kasper Lage, Carol J. Bult, Patricia K. Donahoe	69
5	Maternal periconceptional exposure to cigarette smoking and alcohol consumption and congenital diaphragmatic hernia 2010 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Kristin Caspers, (unknown), Paul A. Romitti, Lixian Sun, Barbara R. Pober, Sonja A. Rasmussen, Wei Yang, Charlotte M. Druschel, (unknown)	20
6	Williams–Beuren Syndrome breakdown → 2010 ·New England Journal of Medicine ·Barbara R. Pober	540
7	Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH 2010 ·American Journal of Medical Genetics Part A ·Sibel Kantarci, Kate G. Ackerman, Meaghan Russell, Mauro Longoni, Carrie Sougnez, Kristin Noonan, Eli Hatchwell, Xiaoyun Zhang, (unknown), Kwame Anyane‐Yeboa, Paul W. Dickman, Jay M. Wilson, Patricia K. Donahoe, Barbara R. Pober	40
8	Deletions of Xp provide evidence for the role of holocytochrome C‐type synthase (HCCS) in congenital diaphragmatic hernia 2010 ·American Journal of Medical Genetics Part A ·(unknown), David Pearson, Gayle Patel, Barbara R. Pober, LaDonna Immken, Sau Wai Cheung, Daryl A. Scott	14
9	Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome 2008 ·Journal of Clinical Investigation ·Barbara R. Pober, Mark D. Johnson, Zsolt Urbán	130
10	Congenital diaphragmatic hernia and associated cardiovascular malformations: Type, frequency, and impact on management 2007 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Angela E. Lin, Barbara R. Pober, Ian Adatia	64
11	Discriminating Power of Localized Three-Dimensional Facial Morphology 2005 ·The American Journal of Human Genetics ·Peter Hammond, Tim J. Hutton, Judith Allanson, Bernard Buxton, Linda Campbell, Jill Clayton‐Smith, Dian Donnai, Annette Karmiloff‐Smith, Kay Metcalfe, Kieran C. Murphy, Michael A. Patton, Barbara R. Pober, Katrina Prescott, Peter Scambler, Adam Shaw, Ann C. M. Smith, Angela Stevens, I. Karen Temple, Raoul C. M. Hennekam, May Tassabehji	118
12	Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome 2005 ·American Journal of Medical Genetics Part A ·Sibel Kantarci, David Casavant, Carlos E. Prada, Matthew Russell, Janice L. B. Byrne, (unknown), Rebecca B. Jennings, Simon M. Manning, Theonia K. Boyd, J. P. Fryns, Lewis B. Holmes, Patricia K. Donahoe, (unknown), Virginia Kimonis, Barbara R. Pober	63
13	Multisystem study of 20 older adults with Williams syndrome 2004 ·American Journal of Medical Genetics Part A ·(unknown), Thomas O. Carpenter, Cheryl Klaiman, (unknown), Joel D. Bregman, Karl Insogna, Robert T. Schultz, Barbara R. Pober	181
14	Fetal stroke 2004 ·Pediatric Neurology ·Koray Özduman, Barbara R. Pober, Patrick D. Barnes, Joshua A. Copel, (unknown), Charles C. Duncan, Laura R. Ment	57
15	FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6 2003 ·American Journal of Medical Genetics Part A ·(unknown), Peining Li, Dongmei Wang, (unknown), Manjunath Nimmakayalu, Mazin Β. Qumsiyeh, Barbara R. Pober	24
16	Genetics of Childhood Disorders: XXVI. Williams Syndrome and Brain–Behavior Relationships 2001 ·Journal of the American Academy of Child & Adolescent Psychiatry ·Robert T. Schultz, David J. Grelotti, Barbara R. Pober	20
17	Identification and Characterization of a Highly Conserved Protein Absent in the Alport Syndrome (A), Mental Retardation (M), Midface Hypoplasia (M), and Elliptocytosis (E) Contiguous Gene Deletion Syndrome (AMME) 1999 ·Genomics ·Francesca Vitelli, Monica Piccini, Francesco Caroli, Brunella Franco, Alessandro Malandrini, Barbara R. Pober, Jón J. Jónsson, Vincenzo Sorrentino, Alessandra Renieri	26
18	FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation 1998 ·Genomics ·Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri	92
19	Type III tracheal agenesis with familial tetralogy of Fallot and absent pulmonary value syndrome 1996 ·American Journal of Medical Genetics ·(unknown), Barbara R. Pober, Lewis B. Holmes	9
20	REPORTING ACCURACY AMONG MOTHERS OF MALFORMED AND NONMALFORMIED INFANTS 1989 ·American Journal of Epidemiology ·Martha M. Werler, Barbara R. Pober, Kathryn Nelson, Lewis B. Holmes	151

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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