David D. Weaver

6.1k citations

117 papers · 3.3k indexed · 1 hit paper · h-index 33

Developmental Biology top 1%
Genetics top 1%
- Genomic variations and chromosomal abnormalities 23
- Congenital Ear and Nasal Anomalies 11
- Connective tissue disorders research 10
- Craniofacial Disorders and Treatments 10
- Genetic Syndromes and Imprinting 9
Urology top 2%
- Urological Disorders and Treatments 10
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics 15
Genetics top 5%
- Genomic variations and chromosomal abnormalities 23
- Congenital Ear and Nasal Anomalies 11
- Connective tissue disorders research 10
- Craniofacial Disorders and Treatments 10
- Genetic Syndromes and Imprinting 9
Surgery
- Congenital Anomalies and Fetal Surgery 11

Co-authors: John M. Opitz James F. Reynolds Jan Nico Bouwes Bavinck Catherine G. Palmer Marilyn J. Bull Gail H. Vance Patricia G. Wheeler Laura Russell
Cited by: Developmental Biology Genetics Urology
Journals: Clinical Genetics (8 papers)Journal of Medical Genetics (4 papers)American Journal of Medical Genetics (33 papers)
Partner nations: United States Canada Spain

In The Last Decade

David D. Weaver

116 papers receiving 3.2k citations

Hit Papers

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Peers

Countries citing papers authored by David D. Weaver

Since Specialization

Citations

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

Fields of papers citing papers by David D. Weaver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David D. Weaver. 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 David D. Weaver. The network helps show where David D. Weaver may publish in the future.

Co-authorship network

The 25 scholars most cited alongside David D. Weaver, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David D. Weaver Line = papers co-authored together David D. Weaver links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The progression of Wiedemann–Steiner syndrome in adulthood and two novel variants in the KMT2A gene American Journal of Medical Genetics Part A ·Said Megahed,Stephen R. Dlouhy,Sarah Backer,Katelyn Payne,David D. Weaver	2018	10
2	Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance Journal of Human Genetics ·Beom Hee Lee,Min Gon Song,Brenden Chen,Hui Mei,Lisa Edelmann,Celia Moss,David D. Weaver,Robert J. Desnick	2015	19
3	Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism Genetics in Medicine ·Andrade Viscarra.,Katie Economidou,Samantha Moldan,Ludwig Van Der Veken,Katherine L. Schumacher,B. Riedel,David D. Weaver,Mary Pell Abernathy,Erik Sebastian,Gail H. Vance	2013	57
4	The use of cone beam computed tomography for the assessment of trichorhinophalangeal syndrome, type I – a case report Journal of Orthodontics ·Ahmed Ghoneima,Le Zhang,James K. Hartsfield,David D. Weaver,Katherine Kula	2013	5
5	Duplication of 18q21.32–q22.3 identified in a stillborn and two relatives with minimal dysmorphic features American Journal of Medical Genetics Part A ·Khadijah Faqih Kasmuddin,靖弘岩須,David D. Weaver,Antje Kabisch,Samantha Moldan,S J Wolgamot,Gail H. Vance	2012	3
6	Report of a mother and daughter with the 12q14 microdeletion syndrome American Journal of Medical Genetics Part A ·D. Gracia,Jill A. Rosenfeld,David D. Weaver	2011	8
7	Cyclopia (synophthalmia) in Smith–Lemli–Opitz syndrome: First reported case and consideration of mechanism American Journal of Medical Genetics Part C Seminars in Medical Genetics ·David D. Weaver,Benjamin D. Solomon,Melissa Adelia Sukardi,Richard I. Kelley,Maximilian Muenke	2010	37
8	A tale of two deletions: A report of two novel 20p13 → pter deletions American Journal of Medical Genetics Part A ·Аліна Юріївна Ковтун,Matthew Pastore,Gail E. Herman,Sarah Alliman,Jill A. Rosenfeld,David D. Weaver	2010	11
9	Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia Journal of Medical Genetics ·Fatima Abidi,Keila Cristina Panesso Camppo,Zhe-Yuan Zhou,David D. Weaver,Richard J. Simensen,Roger E. Stevenson,R. Curtis Rogers,Charles E. Schwartz	2008	76
10	On the spectrum of limb‐body wall complex, exstrophy of the cloaca, and urorectal septum malformation sequence American Journal of Medical Genetics Part A ·Suharsiwi Suharsiwi,David D. Weaver,Philip R. Faught,Gary A. Bellus,Wilfredo Torres‐Martinez	2007	19
11	Vascular-type disruptive defects in fetuses with homozygous α-thalassemia: report of two cases and review of the literature Prenatal Diagnosis ·Margaret P Adam,Jane Chueh,Yasser Y. El‐Sayed,Muhsin Sholeh Said Ahnin,Hannes Vogel,David D. Weaver,H. Eugene Hoyme	2005	19
12	Adults with VATER association: Long‐term prognosis American Journal of Medical Genetics Part A ·Patricia G. Wheeler,David D. Weaver	2005	14
13	Weaver syndrome with neuroblastoma and cardiovascular anomalies American Journal of Medical Genetics ·Tasrial. M.Si,Mediha Ozeren,Rama Jasty,Annelie Brendel,H. B. Robinson,David D. Weaver,M. Michael Cohen	2001	12
14	Hypogonadism and CHARGE association American Journal of Medical Genetics ·Patricia G. Wheeler,Charmian A. Quigley,A. Palano,David D. Weaver	2000	30
15	Weaver syndrome: Autosomal dominant inheritance of the disorder American Journal of Medical Genetics ·Virginia K. Proud,Stephen R. Braddock,Lola Cook,David D. Weaver	1998	22
16	Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome‐like phenotype American Journal of Medical Genetics ·Lino Choez,Wilbur R. Harrison,David D. Weaver,Catherine Palmer,Danielle Marques Raposo Cotia,Joan Overhauser	1994	17
17	Asymmetric and symmetric long bone bowing in two sibs: An apparently new bone dysplasia American Journal of Medical Genetics ·K Shabanam Saiyad,Cynthia A. Moore,John A. Smith,David D. Weaver	1993	5
18	Otopalatodigital syndrome type II associated with omphalocele: Report of three cases American Journal of Medical Genetics ·Katherine Young,Svetlana Baymoldina,Cynthia A. Moore,David D. Weaver	1993	22
19	A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·David D. Weaver,Courtney Williams	1977	3
20	A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly The Journal of Pediatrics ·David D. Weaver,C. Benjamin Graham,I. T. Thomas,David W. Smith	1974	126

About David D. Weaver

David D. Weaver is a scholar working on Genetics, Developmental Biology, Genetics, Urology and Pediatrics, Perinatology and Child Health, having authored 117 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (15 papers), Congenital Anomalies and Fetal Surgery (11 papers), Congenital Ear and Nasal Anomalies (11 papers), Connective tissue disorders research (10 papers), Urological Disorders and Treatments (10 papers), Craniofacial Disorders and Treatments (10 papers) and Genetic Syndromes and Imprinting (9 papers). The work is most often cited by research in Developmental Biology (228 citations), Genetics (1.6k citations), Urology (253 citations), Pediatrics, Perinatology and Child Health (699 citations) and Genetics (322 citations). David D. Weaver has collaborated with scholars based in United States, Canada and Spain. Frequent co-authors include John M. Opitz, James F. Reynolds, Jan Nico Bouwes Bavinck, Catherine G. Palmer, Marilyn J. Bull, Gail H. Vance, Patricia G. Wheeler, Laura Russell, Rebecca S. Wappner and Mark J. Pettenati. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, American Journal of Medical Genetics, Birth Defects Research Part A Clinical and Molecular Teratology and Human 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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