Frances R. Goodman

2.8k citations

20 papers · 1.8k indexed · h-index 18

Molecular Biology top 10%
Genetics top 2%
Developmental Biology top 0.5%
Surgery
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Peter Scambler William Reardon Robin M. Winter Andrea Superti‐Furga Rodger W. Palmer Deborah Shears Matthew L. Warman Douglas P. Mortlock
Topics: Congenital limb and hand anomalies (12 papers)Hedgehog Signaling Pathway Studies (7 papers)Prenatal Screening and Diagnostics (5 papers)
Cited by: Developmental Biology Genetics Molecular Biology
Journals: Proceedings of the National Academy of Sciences The Lancet Nature Genetics
Partner nations: United Kingdom United States India

In The Last Decade

Frances R. Goodman

20 papers receiving 1.7k citations

Peers

Countries citing papers authored by Frances R. Goodman

Since Specialization

Citations

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

Fields of papers citing papers by Frances R. Goodman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frances R. Goodman

This figure shows the co-authorship network connecting the top 25 collaborators of Frances R. Goodman. A scholar is included among the top collaborators of Frances R. Goodman 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 Frances R. Goodman. Frances R. Goodman 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	Mild case of Curry–Jones syndrome 2006 ·Clinical Dysmorphology ·Ellen Thomas,Emma Wakeling,Frances R. Goodman,John C. Dickinson,Christine M Hall,Angela F. Brady	3
2	Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus 2005 ·Prenatal Diagnosis ·Emilia K. Bijlsma,Alida C. Knegt,C. M. Bilardo,Frances R. Goodman	17
3	Congenital abnormalities of body patterning: embryology revisited 2003 ·The Lancet ·Frances R. Goodman	41
4	An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function 2003 ·Development ·Giuliana Caronia,Frances R. Goodman,(unknown),Peter Scambler,Vincenzo Zappavigna	54
5	A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly 2002 ·The American Journal of Human Genetics ·Frances R. Goodman,Frank Majewski,Amanda Collins,Peter Scambler	77
6	Broad phenotypic spectrum caused by an identical heterozygous CDMP‐1 mutation in three unrelated families 2002 ·American Journal of Medical Genetics Part A ·Ravi Savarirayan,Susan M. White,Frances R. Goodman,John M. Graham,Martin B. Delatycki,Ralph S. Lachman,David L. Rimoin,David B. Everman,Matthew L. Warman	45
7	The mutational spectrum of brachydactyly type C 2002 ·American Journal of Medical Genetics ·David B. Everman,Cynthia F. Bartels,Yue Yang,Niranjan Yanamandra,Frances R. Goodman,Roberto Mendoza‐Londono,Ravi Savarirayan,Susan M. White,John M. Graham,Robert Peter Gale,Eva Svarch,William G. Newman,(unknown),Clair A. Francomano,Govindaiah Vinukonda,Lalji Singh,Stuart Morrison,J. Terrig Thomas,Matthew L. Warman	65
8	AHOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome 2002 ·Human Mutation ·Jeffrey W. Innis,Frances R. Goodman,Chiara Bacchelli,Thomas M. Williams,Douglas P. Mortlock,(unknown),Peter Scambler,Wendy McKinnon,Alan E. Guttmacher	53
9	Limb malformations and the human HOX genes 2002 ·American Journal of Medical Genetics ·Frances R. Goodman	157
10	Novel HOXA13 Mutations and the Phenotypic Spectrum of Hand-Foot-Genital Syndrome 2000 ·The American Journal of Human Genetics ·Frances R. Goodman,Chiara Bacchelli,Angela F. Brady,Louise Brueton,Jean‐Pierre Fryns,Douglas P. Mortlock,Jeffrey W. Innis,Lewis B. Holmes,Alan E. Donnenfeld,Murray Feingold,Frits A. Beemer,Raoul C. M. Hennekam,Peter Scambler	189
11	Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis 1999 ·Nature Genetics ·Yaoqin Gong,Deborah Krakow,José Roberto Marcelino,Douglas J. Wilkin,David Chitayat,Riyana Babul‐Hirji,Louanne Hudgins,Cor W. R. J. Cremers,Frans P.M. Cremers,Han G. Brunner,Kent A. Reinker,David L. Rimoin,Daniel H. Cohn,Frances R. Goodman,William Reardon,Michael A. Patton,Clair A. Francomano,Matthew L. Warman	244
12	Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families 1999 ·European Journal of Pediatrics ·Jing Wang,Lewis Spitz,Richard Hayward,Edward M. Kiely,C. Michael Hall,D. O’Donoghue,(unknown),Frances R. Goodman,Peter Scambler,R M Winter,William Reardon	26
13	Two cases with interstitial deletions of chromosome 2 and sex reversal in one 1999 ·American Journal of Medical Genetics ·Anne Slavotinek,(unknown),(unknown),(unknown),Frances R. Goodman,Helen Kingston	45
14	Acromelic Frontonasal Dysostosis 1999 ·American Journal of Medical Genetics ·Sarah F. Slaney,Frances R. Goodman,(unknown),Bryan D. Hall,(unknown),I D Young,Richard Hayward,Barry M. Jones,Arnold L. Christianson,Robin M. Winter	18
15	Acromelic Frontonasal Dysostosis 1999 ·American Journal of Medical Genetics ·Sarah F. Slaney,Frances R. Goodman,(unknown),Bryan D. Hall,(unknown),I D Young,Richard Hayward,Barry M. Jones,Arnold L. Christianson,Robin M. Winter	1
16	Deletions in HOXD13 Segregate with an Identical, Novel Foot Malformation in Two Unrelated Families 1998 ·The American Journal of Human Genetics ·Frances R. Goodman,(unknown),Christine M Hall,William Reardon,Robin Winter,Peter Scambler	79
17	A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis 1998 ·Nature Genetics ·Alison Ross,Víctor L. Ruiz‐Pérez,Yiming Wang,(unknown),Stephen W. Scherer,Sally Ann Lynch,Susan Lindsay,(unknown),Elena Belloni,David I. Wilson,Roy Wadey,Frances R. Goodman,Karen Helene Ørstavik,Tom Monclair,Steve Robson,William Reardon,John Burn,Peter Scambler,(unknown)	204
18	Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis 1998 ·Nature Genetics ·Deborah Shears,(unknown),Frances R. Goodman,Rodger W. Palmer,William Reardon,Andrea Superti‐Furga,Peter Scambler,Robin M. Winter	243
19	Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract 1997 ·Proceedings of the National Academy of Sciences ·Frances R. Goodman,Stefan Mundlos,Yasuteru Muragaki,Dian Donnai,(unknown),Elisabetta Lapi,F. Majewski,Julie McGaughran,C McKeown,William Reardon,Joseph Upton,R M Winter,Bjørn R. Olsen,Peter Scambler	170
20	Liposarcoma of the Spermatic Cord 1991 ·Journal of the Royal Society of Medicine ·Frances R. Goodman,M D Staunton,Helen C. Rees	19

About Frances R. Goodman

Frances R. Goodman is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 20 papers that have together received 1.8k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (12 papers), Hedgehog Signaling Pathway Studies (7 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Developmental Biology (426 citations), Genetics (839 citations) and Molecular Biology (1.2k citations). Frances R. Goodman has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Peter Scambler, William Reardon, Robin M. Winter, Andrea Superti‐Furga, Rodger W. Palmer, Deborah Shears, Matthew L. Warman, Douglas P. Mortlock, Chiara Bacchelli and Jeffrey W. Innis. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Genetics.

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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