Kerry Baldwin Jedele

439 total citations
14 papers, 288 citations indexed

About

Kerry Baldwin Jedele is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Kerry Baldwin Jedele has authored 14 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Surgery. Recurrent topics in Kerry Baldwin Jedele's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Kerry Baldwin Jedele is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Kerry Baldwin Jedele collaborates with scholars based in Germany, United States and Austria. Kerry Baldwin Jedele's co-authors include Virginia V. Michels, Elke Holinski‐Feder, Robert Feldt, Francisco J. Puga, Alfons Meindl, Oliver Brandau, Bernd H. Belohradsky, Smith Rjh, Michael Weiss and Mauno Vihinen and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and European Journal of Human Genetics.

In The Last Decade

Kerry Baldwin Jedele

14 papers receiving 282 citations

Peers

Countries citing papers authored by Kerry Baldwin Jedele

Since Specialization

Citations

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

Fields of papers citing papers by Kerry Baldwin Jedele

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerry Baldwin Jedele. 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 Kerry Baldwin Jedele. The network helps show where Kerry Baldwin Jedele may publish in the future.

Co-authorship network of co-authors of Kerry Baldwin Jedele

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Compound Heterozygosity for MSH6 Mutations in a Pediatric Lymphoma Patient 2009 ·Journal of Pediatric Hematology/Oncology ·(unknown), Hayley Born, Robert S. Ettinger, (unknown), Kerry Baldwin Jedele	11
2	The Overlapping Spectrum of Rett and Angelman Syndromes: A Clinical Review 2007 ·Seminars in Pediatric Neurology ·Kerry Baldwin Jedele	39
3	MRX42: Two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation 2002 ·American Journal of Medical Genetics ·Astrid Golla, Imma Rost, Kerry Baldwin Jedele, (unknown), Jan Murken, Elke Holinski‐Feder	2
4	Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3) 2000 ·The American Journal of Human Genetics ·Elke Holinski‐Feder, Edwin Reyniers, Sabine Uhrig, Astrid Golla, J. Wauters, Peter M. Kroisel, Paul Bossuyt, Imma Rost, Kerry Baldwin Jedele, (unknown), (unknown), Dieter B. Wildenauer, Michael R. Speicher, (unknown), Thomas Meitinger, R. Frank Kooy	43
5	Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region 1999 ·American Journal of Medical Genetics ·Elke Holinski‐Feder, (unknown), Olaf Rittinger, Kerry Baldwin Jedele, (unknown), C Lenski, Jan Murken, Astrid Golla	9
6	Mutation Screening of the BTK Gene in 56 Families With X-Linked Agammaglobulinemia (XLA): 47 Unique Mutations Without Correlation to Clinical Course 1998 ·PEDIATRICS ·Elke Holinski‐Feder, Michael Weiss, Oliver Brandau, Kerry Baldwin Jedele, Beston F. Nore, (unknown), Mauno Vihinen, Stevan R. Hubbard, Bernd H. Belohradsky, Smith Rjh, Alfons Meindl	87
7	Spinal and bulbar muscular atrophy (SBMA): Somatic stability of an expanded CAG repeat in fetal tissues 1998 ·Clinical Genetics ·Kerry Baldwin Jedele, Dagmar Wahl, (unknown), Antje Wirtz, Jan Murken, Elke Holinski‐Feder	5
8	UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2 1998 ·European Journal of Human Genetics ·Oliver Brandau, Gerald Nyakatura, Kerry Baldwin Jedele, Matthias Platzer, Helene Achatz, Mark T. Ross, Jan Murken, André Rosenthal, Alfons Meindl	6
9	Large Intergenerational Variation in Age of Onset in Two Young Patients With Huntington's Disease Presenting as Dyskinesia 1997 ·PEDIATRICS ·Elke Holinski‐Feder, Kerry Baldwin Jedele, Konstanze Hörtnagel, (unknown), Alfons Meindl, Claudia Trenkwalder	2
10	Discordant monozygotic twins with the Schimmelpenning‐Feuerstein‐Mims syndrome 1996 ·Clinical Genetics ·Hermann Dieter Schworm, Kerry Baldwin Jedele, (unknown), Konstanze Hörtnagel, Günter Rudolph, K.‐P. Boergen, Anselm Kampik, Thomas Meitinger	17
11	Linkage of nonspecific X‐linked mental retardation to Xq21.31 1992 ·American Journal of Medical Genetics ·Kerry Baldwin Jedele, Virginia V. Michels, Daniel J. Schaid, (unknown), (unknown)	12
12	Velo-Cardio-Facial Syndrome Associated With Ventricular Septal Defect, Pulmonary Atresia, and Hypoplastic Pulmonary Arteries 1992 ·PEDIATRICS ·Kerry Baldwin Jedele, Virginia V. Michels, Francisco J. Puga, Robert Feldt	42
13	Familial dermographism 1991 ·American Journal of Medical Genetics ·Kerry Baldwin Jedele, Virginia V. Michels	8
14	Frequency of congenital heart defects in patients with hemophilia 1990 ·American Journal of Medical Genetics ·Kerry Baldwin Jedele, Virginia V. Michels, Hymie Gordon, Gerald S. Gilchrist	5

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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