Richard H. Finnell

Also affiliated with Baylor College of Medicine, Baylor Genetics

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 6%percentile

0.224Author DataRank

Indexed papers

3in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082

Top 62%

0.224DataRank

Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Papers

Driven by 51 papers — median percentile 19. Top paper: “Excess folic acid intake increases DNA de novo point mutations”.

Excess folic acid intake increases DNA de novo point mutations

Cell Discovery(2023)10.1038/s41421-022-00512-0

N/A

1.6DataRank · unranked

40 citations

Jianfeng Xu, Ying Lin, Robert M. Cabrera, Qiuying Chen, Chaofan Zhang +10 more

Behavioral Outcomes and Neurodevelopmental Disorders Among Children of Women With Epilepsy

JAMA Neurology(2023)10.1001/jamaneurol.2023.4315

N/A

0.464DataRank · unranked

21 citations

Kimford J. Meador, David W. Loring, Abigail G. Matthews, Carrie Brown, Chelsea P. Robalino +95 more

The contribution of de novo coding mutations to meningomyelocele

Nature(2025)10.1038/s41586-025-08676-x

N/A

0.396DataRank · unranked

13 citations

Ashna Nisal, Isaac Tang, Chanjae Lee, Ishani Jhamb, Cassidy Wallace +74 more

Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63185

N/A

0.292DataRank · unranked

6 citations

Aniko Sabo, Lynn M. Almli, Mary M. Jenkins, Wendy N. Nembhard, A. J. Agopian +28 more

CIC missense variants contribute to susceptibility for spina bifida

Human Mutation(2022)10.1002/humu.24460

N/A

0.292DataRank · unranked

6 citations

Xuanye Cao, Vanessa Aguiar‐Pulido, Wei Yang, Menuka Karki, Paula Andrea Pimienta Ramírez +9 more

Exome sequencing identifies variants in infants with sacral agenesis

Birth Defects Research(2022)10.1002/bdr2.1987

N/A

0.241DataRank · unranked

4 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +21 more

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082

Top 62%

0.224DataRank

Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Maternal–fetal metabolic gene–gene interactions and risk of neural tube defects

UNC Libraries(2020)10.17615/qvww-zx65

N/A

0DataRank · unranked

0 citations

Mark A. Canfield, Gary M. Shaw, Laura E. Mitchell, Huiping Zhu, Andrew F. Olshan +2 more

Gene Environment Interactions in the Etiology of Neural Tube Defects

Frontiers in Genetics(2021)10.3389/fgene.2021.659612

N/A

0DataRank · unranked

108 citations

Carlo Donato Caiaffa, Sung‐Eun Kim, Yunping Lei, John Steele, Xuanye Cao +5 more

Actuation enhances patterning in human neural tube organoids

Nature Communications(2021)10.1038/s41467-021-22952-0

N/A

0DataRank · unranked

92 citations

Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal +14 more

Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects

Epigenetics(2021)10.1080/15592294.2021.1878725

N/A

0DataRank · unranked

19 citations

Xinyuan Lai, Kuanhui Xiang, Xiao Han, Shengju Yin, Robert M. Cabrera +7 more

Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.641831

N/A

0DataRank · unranked

19 citations

Xuanye Cao, Yongyan Chen, Lei Jin, Zhiwen Li, Xiao Han +8 more

Wnt1 Lineage Specific Deletion of Gpr161 Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal Development

Frontiers in Genetics(2021)10.3389/fgene.2021.761418

N/A

0DataRank · unranked

13 citations

Karla Robles-Lopez, Xuanye Cao, Kristyn Liu, Pooja J. Chothani, Nikitha Bhavani +5 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62439

N/A

0DataRank · unranked

8 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +17 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

PLoS Genetics(2021)10.1371/journal.pgen.1009413

N/A

0DataRank · unranked

4 citations

Emine Bircan, Xinyu Tang, Mohammed S. Orloff, Charlotte A. Hobbs, Marilyn L. Browne +11 more

Multimodal imaging system combining optical coherence tomography and Brillouin microscopy for neural tube imaging

Optics Letters(2022)10.1364/ol.453996

N/A

0DataRank · unranked

29 citations

Manmohan Singh, Alexander W. Schill, Jitao Zhang, Christian Zevallos-Delgado, Behzad Khajavi +5 more

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62874

N/A

0DataRank · unranked

8 citations

Wei Yang, Yuejun Wang, Chen Ma, Cynthia J. Curry, Daniel McGoldrick +21 more

KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

Biology(2022)10.3390/biology12010074

N/A

0DataRank · unranked

6 citations

Xuanye Cao, Robert M. Cabrera, Paula Andrea Pimienta Ramírez, Cuilian Zhang, V. Ramaekers +3 more

Associations between maternal reports of periconceptional fever from miscellaneous causes and structural birth defects

Birth Defects Research(2022)10.1002/bdr2.2068

N/A

0DataRank · unranked

4 citations

Lorenzo D. Botto, Sarah C. Tinker, Mark A. Canfield, Richard H. Finnell, M. Shayne Gallaway +6 more

Maternal metabolism influences neural tube closure

Trends in Endocrinology and Metabolism(2023)10.1016/j.tem.2023.06.005

N/A

0DataRank · unranked

20 citations

Richard H. Finnell, Ronald J. Parchem, Rachel A. Keuls

A mutation in TBXT causes congenital vertebral malformations in humans and mice

Journal of genetics and genomics/Journal of Genetics and Genomics(2023)10.1016/j.jgg.2023.09.009

N/A

0DataRank · unranked

10 citations

Yunping Lei, Yajun Yang, Chennan Liu, Lele Kuang, Jin Li +4 more

Folate regulation of planar cell polarity pathway and F‐actin through folate receptor alpha

The FASEB Journal(2023)10.1096/fj.202300202r

N/A

0DataRank · unranked

7 citations

Xuanye Cao, Robert M. Cabrera, Paula Andrea Pimienta Ramírez, Ying Lin, Bogdan J. Wlodarczyk +4 more

Pax3 lineage-specific deletion of Gpr161 is associated with spinal neural tube and craniofacial malformations during embryonic development

Disease Models & Mechanisms(2023)10.1242/dmm.050277

N/A

0DataRank · unranked

5 citations

Pooja J. Chothani, Rehana Shaik, W. O. Pollard, Richard H. Finnell, Sung‐Eun Kim

Pax3 lineage-specific deletion of Gpr161 is associated with spinal neural tube and craniofacial malformations during embryonic development

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.07.548129

N/A

0DataRank · unranked

1 citations

Pooja J. Chothani, Rehana Shaik, W. O. Pollard, Richard H. Finnell, Sung‐Eun Kim

Aberrant tissue stiffness impairs neural tube development in Mthfd1l mutant mouse embryos

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.04.552024

N/A

0DataRank · unranked

0 citations

Carlo Donato Caiaffa, Bogdan J. Wlodarczyk, Manmohan Singh, Alexander Schill, John Steele +5 more

Disruption of Fuz in mouse embryos generates hypoplastic hindbrain development and reduced cranial nerve ganglia

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.04.552068

N/A

0DataRank · unranked

0 citations

Yogeshwari S. Ambekar, Manmohan Singh, Ying Lin, Bogdan J. Wlodarczyk, Salavat R. Aglyamov +4 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

N/A

0DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

Dolutegravir induces FOLR1 expression during brain organoid development

Frontiers in Molecular Neuroscience(2024)10.3389/fnmol.2024.1394058

N/A

0DataRank · unranked

14 citations

Gabriel Tukeman, Christian Zevallos‐Delgado, Yogeshwari S. Ambekar, Taye Mekonnen, Manmohan Singh +9 more

Mechanisms of neurodevelopmental toxicity of topiramate

Critical Reviews in Toxicology(2024)10.1080/10408444.2024.2368552

N/A

0DataRank · unranked

8 citations

Vaishnav Krishnan, Richard H. Finnell, John Steele

Optical coherence tomography-guided Brillouin microscopy highlights regional tissue stiffness differences during anterior neural tube closure in the Mthfd1l murine mutant

Development(2024)10.1242/dev.202475

N/A

0DataRank · unranked

4 citations

Carlo Donato Caiaffa, Bogdan J. Wlodarczyk, Manmohan Singh, Alexander Schill, John Steele +6 more

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101851

N/A

0DataRank · unranked

4 citations

Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai +72 more

Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study

Birth Defects Research(2024)10.1002/bdr2.2384

N/A

0DataRank · unranked

2 citations

Kristin J. Moore, K.E. North, Tania A. Desrosiers, Suzan L. Carmichael, Janson J. White +19 more

Integrative computational analyses implicate regulatory genomic elements contributing to spina bifida

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101894

N/A

0DataRank · unranked

2 citations

Vanessa Aguiar‐Pulido, Gaurav Thareja, Karsten Suhre, Olivier Elemento, Richard H. Finnell +2 more

Disruption of Fuz in mouse embryos generates hypoplastic hindbrain development and reduced cranial nerve ganglia

Developmental Dynamics(2024)10.1002/dvdy.702

N/A

0DataRank · unranked

1 citations

Yogeshwari S. Ambekar, Manmohan Singh, Ying Lin, Bogdan J. Wlodarczyk, Salavat R. Aglyamov +4 more

Linkage between Fuz and Gpr161 genes regulates sonic hedgehog signaling during mouse neural tube development

Development(2024)10.1242/dev.202705

N/A

0DataRank · unranked

1 citations

Hyun-Yi Kim, Bogdan J. Wlodarczyk, Richard H. Finnell, Sung‐Eun Kim

Epigenetic regulation by TET1 in gene-environmental interactions influencing susceptibility to congenital malformations

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.21.581196

N/A

0DataRank · unranked

2 citations

Lehua Chen, Spyridon Champeris Tsaniras, Wannes Brangers, Qiuying Chen, Mariana Schroiff +9 more

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia

UNC Libraries(2024)10.17615/94re-8d47

N/A

0DataRank · unranked

0 citations

Wendy N. Nembhard, Paul A. Romitti, Marcia L. Feldkamp, Y.J. Wang, Andrew F. Olshan +22 more

Exome sequencing identifies variants in infants with sacral agenesis

UNC Libraries(2024)10.17615/sevc-bn40

N/A

0DataRank · unranked

0 citations

Faith Pangilinan, Andrew F. Olshan, Richard H. Finnell, Martha M. Werler, Cynthia A. Moore +24 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

UNC Libraries(2024)10.17615/4645-7p40

N/A

0DataRank · unranked

0 citations

Marcia L. Feldkamp, Nathan Pankratz, Lawrence C. Brody, John W. Lane, K.M. Conway +18 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

UNC Libraries(2024)10.17615/4h14-yj71

N/A

0DataRank · unranked

0 citations

Jianlin Li, Paul A. Romitti, Wendy N. Nembhard, Andrew F. Olshan, Marilyn L. Browne +11 more

Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data

UNC Libraries(2024)10.17615/j34v-vj41

Top 100%

0DataRank

Top 100%0 citations

Wendy N. Nembhard, Shiran Shapira, Andrew F. Olshan, Elizabeth Blue, Nanette M. Nascone‐Yoder +27 more

Folate receptor β performs an immune checkpoint function in activated macrophages

Frontiers in Immunology(2025)10.3389/fimmu.2025.1638907

N/A

0DataRank · unranked

2 citations

Md. Yusuf Al-Amin, Sagar M. Utturkar, Rina Jiang, Gregory M. Cresswell, Rami A. Alfar +8 more

Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Defects through Dysregulation of DNA Methylation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.27.656260

N/A

0DataRank · unranked

1 citations

Colin Custers, Wannes Brangers, Riet Cornelis, Spyridon Champeris Tsaniras, Kobe De Ridder +8 more

Loss ofRAD9Bimpairs early neural development and contributes to the risk for human spina bifida

Human Mutation(2020)10.1002/humu.23969

N/A

0DataRank · unranked

19 citations

Tian Tian, John Steele, Robert M. Cabrera, Vanessa Aguiar‐Pulido, Shruti Wadhwa +12 more

Associations of arsenic exposure and folate in maternal leukocyte DNA methylation: a case-control study of mothers with spina-bifida affected children

Environmental Health(2026)10.1186/s12940-025-01254-8

N/A

0DataRank · unranked

0 citations

Anne K. Bozack, Bernardo Lemos, Tabitha Lumour-Mensah, Sudipta Kumar Mukherjee, Shekh Muhammad Ekramullah +8 more

FKBP8 variants are risk factors for spina bifida

Human Molecular Genetics(2020)10.1093/hmg/ddaa211

N/A

0DataRank · unranked

8 citations

Xuanye Cao, Sung‐Eun Kim, Ying Lin, John Steele, Robert M. Cabrera +13 more

CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106987

N/A

0DataRank · unranked

25 citations

Annika Wolf, Sung‐Eun Kim, Robert M. Cabrera, Bogdan Włodarczyk, Huiping Zhu +9 more

MiR-302 Regulates Glycolysis to Control Cell-Cycle during Neural Tube Closure

International Journal of Molecular Sciences(2020)10.3390/ijms21207534

N/A

0DataRank · unranked

25 citations

Karin Kojima, Brittney Lozzi, John Steele, Qiuying Chen, Steven S. Gross +3 more

Approaches to studying the genomic architecture of complex birth defects

Prenatal Diagnosis(2020)10.1002/pd.5760

N/A

0DataRank · unranked

8 citations

Xuanye Cao, Robert M. Cabrera, Yunping Lei, Richard H. Finnell, Toluwani Taiwo

Actuation Enhances Patterning in Human Neural Tube Organoids

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.22.308411

N/A

0DataRank · unranked

9 citations

Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal +12 more

Diabetes and Obesity-Related Genes and the Risk of Neural Tube Defects in the National Birth Defects Prevention Study

UNC Libraries(2020)10.17615/9gv2-gf96

N/A

0DataRank · unranked

0 citations

Huiping Zhu, Mark A. Canfield, Claudia Chapa, A. J. Agopian, D. Kim Waller +6 more

Richard H. Finnell

Indexed papers

Top data-sharing exemplar

Papers