Robert S. Wildin

4.6k total citations · 2 hit papers
31 papers, 3.0k citations indexed

About

Robert S. Wildin is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, Robert S. Wildin has authored 31 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 11 papers in Immunology and 9 papers in Molecular Biology. Recurrent topics in Robert S. Wildin's work include Immune Cell Function and Interaction (7 papers), Diabetes and associated disorders (7 papers) and T-cell and B-cell Immunology (7 papers). Robert S. Wildin is often cited by papers focused on Immune Cell Function and Interaction (7 papers), Diabetes and associated disorders (7 papers) and T-cell and B-cell Immunology (7 papers). Robert S. Wildin collaborates with scholars based in United States, Israel and France. Robert S. Wildin's co-authors include Ephrat Levy‐Lahad, Jean‐Laurent Casanova, Jane Peake, Mary E. Brunkow, Massimo Mazzella, Sean Proll, F. Dagna Bricarelli, Geoffrey C Byrne, Olivier Goulet and Fred Ramsdell and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Robert S. Wildin

30 papers receiving 2.9k 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.

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

2001 1.4k citations Robert S. Wildin, Fred Ramsdell et al. Nature Genetics profile →
Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

2002 517 citations Robert S. Wildin et al. Journal of Medical Genetics profile →

Peers

Countries citing papers authored by Robert S. Wildin

Since Specialization

Citations

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

Fields of papers citing papers by Robert S. Wildin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert S. Wildin. 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 Robert S. Wildin. The network helps show where Robert S. Wildin may publish in the future.

Co-authorship network of co-authors of Robert S. Wildin

This figure shows the co-authorship network connecting the top 25 collaborators of Robert S. Wildin. A scholar is included among the top collaborators of Robert S. Wildin 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 Robert S. Wildin. Robert S. Wildin 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	Cost Effectiveness of Genomic Population Health Screening in Adults: A Review of Modeling Studies and Future Directions 2024 ·The Journal of Applied Laboratory Medicine ·Robert S. Wildin	1
2	Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening 2023 ·Journal of Community Genetics ·(unknown), (unknown), Robert S. Wildin	2
3	Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing Panel 2022 ·Frontiers in Genetics ·Robert S. Wildin, (unknown), (unknown), Thomas C. Peterson, Debra G. B. Leonard	5
4	Modernizing family health history: achievable strategies to reduce implementation gaps 2021 ·Journal of Community Genetics ·Robert S. Wildin, Donna J. Messersmith, Elisa J. F. Houwink	12
5	Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis 2016 ·JCI Insight ·(unknown), (unknown), Ying Qiao, Rita Colnaghi, (unknown), Diana Alcantara, Christopher Dunham, Jiadi Wen, Robert S. Wildin, Małgorzata J.M. Nowaczyk, (unknown), Anna Lehman, Bruno Maranda, Sally Martell, Xianghong Shan, M. E. Suzanne Lewis, Mark O’Driscoll, Cheryl Y. Gregory‐Evans, Evica Rajcan‐Separovic	23
6	Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes 2013 ·Human Mutation ·Ying Qiao, Kajari Mondal, Valentina Trapani, Jiadi Wen, Gillian Carpenter, Robert S. Wildin, E. Magda Price, Richard J. Gibbons, (unknown), (unknown), Barbara R. DuPont, Sally Martell, M. E. Suzanne Lewis, Wendy P. Robinson, Mark O’Driscoll, Federica I. Wolf, Michael E. Zwick, Evica Rajcan‐Separovic	8
7	A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33 2010 ·PLoS ONE ·Ryan N. Traylor, Damien L. Bruno, Trent Burgess, Robert S. Wildin, (unknown), Devika Ganesamoorthy, David J. Amor, Matthew F. Hunter, Michael S. Caplan, Jill A. Rosenfeld, Aaron Theisen, Beth S. Torchia, Lisa G. Shaffer, Blake C. Ballif, Howard R. Slater	21
8	Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm 2005 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Michael G. Brown, Helen J. Lawce, Joseph Gilhooly, Robert S. Wildin, Leesa M. Linck, R. Ellen Magenis, De‐Ann M. Pillers	21
9	IPEX and FOXP3: Clinical and research perspectives 2005 ·Journal of Autoimmunity ·Robert S. Wildin, António A. Freitas	115
10	Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) 2004 ·Clinical & Experimental Immunology ·A C Bakke, (unknown), Robert S. Wildin	21
11	Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome breakdown → 2002 ·Journal of Medical Genetics ·Robert S. Wildin, (unknown), (unknown)	517
12	Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome 2001 ·The Journal of Pediatrics ·Ephrat Levy‐Lahad, Robert S. Wildin	56
13	X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy breakdown → 2001 ·Nature Genetics ·Robert S. Wildin, Fred Ramsdell, Jane Peake, Francesca Faravelli, Jean‐Laurent Casanova, Neil R.M. Buist, Ephrat Levy‐Lahad, Massimo Mazzella, Olivier Goulet, L Perroni, F. Dagna Bricarelli, Geoffrey C Byrne, (unknown), Sean Proll, Mark W. Appleby, Mary E. Brunkow	1422
14	Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation 2001 ·New England Journal of Medicine ·Olivier Baud, Olivier Goulet, Danielle Canioni, Françoise Le Deist, Isabelle Radford, D Rieu, Sophie Dupuis‐Girod, Nadine Cerf–Bensussan, Marina Cavazzana, Nicole Brousse, Alain Fischer, Christine Rivet, Christine Bodemer, Robert S. Wildin, Jean‐Laurent Casanova	172
15	Regulation of Src-family protein tyrosine kinase transcription during lymphocyte ontogeny 1999 ·Molecular Immunology ·Nancy S. Longo, Xin Wang, Robert S. Wildin, Kristin M. Abraham	8
16	AVPR2 variants and V2 vasopressin receptor function in nephrogenic diabetes insipidus 1998 ·Kidney International ·Robert S. Wildin, David Cogdell, (unknown)	31
17	Correlation of linkage data with phenotype in eight families with Stickler syndrome 1998 ·American Journal of Medical Genetics ·Douglas J. Wilkin, Geert Mortier, (unknown), Marilyn C. Jones, Anne De Paepe, Mordechai Shohat, Robert S. Wildin, Rena E. Falk, Daniel H. Cohn	4
18	Functional dissection of the murine lck distal promoter 1995 ·The Journal of Immunology ·Robert S. Wildin, (unknown), Katherine A. Forbush, Roger M. Perlmutter	56
19	Developmental regulation of lck gene expression in T lymphocytes. 1991 ·The Journal of Experimental Medicine ·Robert S. Wildin, Alex M. Garvin, Shashi Singh Pawar, David B. Lewis, Kristin M. Abraham, Katherine A. Forbush, Steven F. Ziegler, James M. Allen, Roger M. Perlmutter	108
20	Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase 1982 ·Nature ·(unknown), Robert S. Wildin, T S Su	56

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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